NEET MDS – How to prepare for Operative Dentistry

In the NEET MDS Preparation process, the students need to study the previous year exams thoroughly and identify the important topics. This article sheds light on Operative Dentistry & the list of Questions MERITERS experts will answer that are essential for an effective and efficient preparation:

  1. What is the subject wise Weightage?
  2. Which Books to refer?
  3. How much Time should be allocated to the subject?
  4. How much Time should be allocated to each Topic?
  5. How many times should the subject be Revised?
  6. What is the Ideal time to Start the subject?
  7. What are the Important Topics for NEET MDS?
  8. Types of Questions asked?

What is the subject wise Weightage?

10-13/240 Questions (5%)

Standard Books to Refer:

Sturdevant’s Art & Science of Operative Dentistry – E-Book

Author : V Gopikrishna

INR 1,338 Buy on Amazon

Sturdevant’s Art and Science of Operative Dentistry 

Author : Andre V. Ritter DDS MS 

INR 7,595 Buy on Amazon

How much Time should be allocated for the Subject?

  • Theory reading – 1-2 Days
  • MCQ Practice- 1 week


How much Time should be allocated to each Topic?

  • Theory reading – 2-3 Hours
  • MCQ Practice-  6-8 Hours


How many Times should the subject be Revised?

  • 4-6 times revision is required


What is the Ideal time to Start the subject?

  • 4th quarter of the preparation 
  • After completing 17-19 subjects

Operative Dentistry – Important Topics

UnitMost Important Topics
CariologyDiagnosis and Treatment planning
Operator Positions
Microbiology of Caries
Classification of Caries- GV Black, Root caries, Caries cone
Histo-pathological changes of Enamel and Dentin
Diagnosis of Caries
After Restoration Procedures
Infection controlOccupational Safety and Health ActAerosols and UltrasonicsClassification of Medical, Surgical and Dental InstrumentsSterilization
 Dental AdhesionEnamel and dentin bonding systems
Direct filling goldClassificationManipulationPrinciples of tooth preparation
CompositesComposition and classificationCavity preparationPolymerization of composites
AmalgamClassificationPin retained amalgam restorationsMercury toxicityTrituration
Caries and Cavity PreparationCariologyTooth preparation
Sterlization and IsolationMoist and dry heat sterilization, ETOX gasRubber damMatrices
Direct Filling GoldTypes of Direct Filling GoldCavosurface MarginCohesive GoldDegassingCondensation and CompactionProperties of Gold
Cast Gold Restorations, Inlays, OnlaysIndications and Contraindications
Principles of Tooth Preparations
Finish Lines and Cavosurface Margins
Sprue
Porosities
CAD –CAM
Functional Cusp Bevel
Biomechanical PrinciplesCavity Preparation, Smear Layer
Rubber Dam in Detail
Separators/ Wedges/ Matrices
Gingival Retraction
Debridement, Polishing Agents
Pulp Protection, Air Abrasion
UltraSonics and Lasers in Cavity Preparation
Walls of Cavity/ Line Angles/ Point Angles
Outline Form, Resistance Form
Retention Form, Bevels
Depth Of Cavity, Ferrules
InstrumentationHand Cutting Instruments
Instrument Formula
GMT, Angle Former
Hatchets, Angles of Dental Bur
Efficiency of Burs
Carbide/ Diamond/ Stainless Steel Burs
Amalgam RestorationsIndications/ Contraindications of Amalgam Restorations
Father of Amalgam
Properties of Amalgam
Creep, Phases of Amalgam
Microleakage, Delayed Expansion
Overhangs, Trituration
Eame’s Technique
Burnishing, Condensation
Mercuric Toxicity
Pin Retained Amalgam Restorations
Types of Pins, Thread Mate System
Bonded Amalgam Restorations
Tooth Colored RestorationsAdvantages/Disadvantages
Indications/Contraindications
Acid Etching
Skipping Effect
Dentin Conditioner
Primers and Adhesive Resin Generations
Fillers in Composites
C-Factor
Margins and Cavosurface Angles
Shade Determination
BIS-GMA
Compomers
Giomers
Porcelain Restorations
Other topicsDentin Hypersensitivity
Mahler Scale
Box and Tunnel Restorations
Veneers and Laminates
Bonding Agents

What Type of Questions were asked in NEET?

1. Single best answer

  • Case Based
  • Fact Based (Memory)
  • Concept based
  • Numerical/Value Based

2. Image based questions

3. True or false type questions

Please watch the above featured video for more detailed explanation about this article.

We hope this blog will assist you in preparing this subject meticulously for MDS entrance exams.
Prepare judiciously..


SOURCE: MERITERS!!

NEET MDS – How To Prepare For Fixed Partial Denture?

Fixed Partial Denture is a part of Prosthodontics which is considered to be an important and extensive subject in NEET MDS. At least 2-5 questions from Fixed Partial Denture can be expected in the NEET PG Exam. This subject requires a thorough study of exam pattern and the ability to recognize the important topics.

We have compiled a list of Questions in this article, which MERITERS experts will answer and are very essential for an effective and efficient preparation:

  1. What is the subject wise Weightage?
  2. Which Books to refer?
  3. How much Time should be allocated to the subject?
  4. How much Time should be allocated to each Topic?
  5. How many times should the subject be Revised?
  6. What is the Ideal time to Start the subject?
  7. What are the Important Topics for NEET MDS?
  8. Types of Questions asked?

What is the subject wise Weightage?

Standard books to Refer?

FUNDAMENTALS OF FIXED PROSTHODONTICS

Author : SHILLINGBURG H.T

INR 2,680 Buy on Amazon

Contemporary Fixed Prosthodontics

Author : Stephen F. Rosenstiel BDS MSD 

INR 950 Buy on Amazon

How much Time should be allocated for the Subject?

  • Theory reading – 1-2 Days
  • MCQ Practice- 1 week


How much Time should be allocated to each Topic?

  • Theory reading – 2-3 Hours
  • MCQ Practice-  6-8 Hours


How many Times should the subject be Revised?

  • 4-6 times revision is required


What is the Ideal time to Start the subject?

  • 4th quarter of the preparation 
  • After completing 17-19 subjects

Fixed Partial Denture – Important Topics

UNIT NAMEMOST IMPORTANT TOPICS
Diagnosis and treatment planningDiagnostic Casts
Indications, Contra Indications
Pontic Designs, Trauma from Occlusion
Mouth Preparation
Cantilever
Retainers and connectorsComponents of FPD
Indications for Non-Rigid FPD
Partial Veneer Crowns Indications and Contra Indications Porcelain Jacket Crown
AbutmentsAnte’s Law
Optimum Crown-Root Ratio
Root Surface Area of Each Tooth
PonticsTypes of Pontics and their Important Features
Gingival End of Pontic
Pontics Suitable for Anterior Region
Pontics Suitable for Posterior Region
Technical considerationsForces acting on Abutment Tooth
Structural Durability
Retention, Taper
Freedom of Displacement
Reduction, Types of Crowns
Three-Quarter Crowns
Retentive Grooves
Porcelain Jacket Crown
Indications of Laminates
Metal Ceramic Restorations
Types of Finish Lines and their Indications
Pier Abutment
Lost Salt Technique
Maryland Bridge
Rochette Bridge
Virginia Bridge
MiscellaneousGingival Retraction
Failure of Abutment
Cementation and post- cementation problemsThickness of Luting Cement
Occlusal Disharmony
Occlusal considerationsVariation between Centric Relation and Maximum Intercuspation
Canine Protected Occlusion
Bennett Shift
Bennett Movement
Working Side
Non-Working Side
Selective Grinding
Beyron’s Point
Types of Bone Quality
Obturators

What Type of Questions were asked in NEET?

1. Single best answer

  • Case Based
  • Fact Based (Memory)
  • Concept based
  • Numerical/Value Based

2. Image based questions

3. True or false type questions

Please watch the above featured video for more detailed explanation about this article.

We hope this blog will assist you in preparing this subject meticulously for MDS entrance exams.
Prepare judiciously..


SOURCE: MERITERS!!

Viral Childhood Exanthems

  • Viral rashes are often caused by immune reactions to the virus and cell damage caused by the virus.
  • A key bacterial cause of rash is Streptococcus pyogenes, which causes Scarlet Fever.

Helpful distinguishers between the viral exanthems:

  • We can categorize them by the initial location and pattern of the rash.
    – Three viral exanthems tend to initiate on the face:
    Measles, rubella, and erythema infectiosum.
    – Chickenpox arises on the face/scalp and trunk.
    – Roseola infantum typically first appears on the trunk
    – Hand, Foot, and Mouth disease produces rash on the hands and feet, in the mouth.

Be aware that these are meant to be helpful generalizations, and may not always hold true; for example, hand, foot, and mouth disease can also produce rash on the buttocks.

  • Rash types:
    – Multiple rash types can exist at once.
    – Macules are flat, colored spots on the skin.
    – Papules are solid, raised areas; larger papules are called nodules.
    – Vesicular rashes comprise raised “pockets” of fluid in the skin.
  • The timing of the rash and presence of other symptoms can also help distinguish among the exanthems.
    – For example, some infections are associated with fever, malaise, and respiratory symptoms.
    – Knowing the time lapse between virus introduction and symptom appearance can also help, although the incubation periods of the various viruses often overlap and may include a wide range.

VIRAL EXANTHEMA

Hand, foot, and mouth disease:

  • Usually caused by Coxsackievirus A.
  • Average incubation period of 3-6 days.
  • Most common in children younger than 5.
  • As its name suggests, hand, foot, and mouth disease is characterized by a rash that can be macular, maculopapular, or vesicular on the hands, feet, and in and around the mouth.

Erythema infectiousum, aka, Fifth Disease

  • Caused by Parvovirus B19.
  • Average incubation period of 7 days
  • Tends to affect children 5-15 years old.
  • Initial symptoms can include fever, runny nose, headache; diarrhea is also possible.
  • These flu-like symtpoms are followed by a malar facial rash that spreads to the trunk and extremities.
    – Facial rash takes on a characteristic “slapped cheeks” pattern, whereas the rash on the extremities often comprises maculopapular rash in a “lacy” pattern.

Roseola infantum, aka, exanthema subitum

  • Most commonly caused by Human Herpes Virus 6, and sometimes Human Herpes Virus 7.
  • Roseola infantum is also sometimes called “6th disease”, because it was the 6th exanthema identified (erythema infectiosum was the fifth).
  • Average incubation period is 9 days.
  • Although disease can occur in a wide range of ages, it most commonly affects children younger than 2 years old.
  • Initial symptoms include a very high fever (exceeding 104 degrees Fahrenheit/40 degrees Celsius).
    – The fever lasts approximately 3 days, which is why Roseola infantum is sometimes called “3-Day Fever”.
  • Macular or maculopapular “blanching rash” arises first on the trunk.
    – “Blanching rash” means that when the skin is pressed upon, often with a clear glass, the rash fades from red to pale.
  • Another common finding are red uvulopalatoglossal spots, aka, Nagayama spots,.
  • A range of other symptoms, including gastrointestinal, respiratory, ocular, and auditory problems, can occur.
  • Febrile seizures are a common complication in roseola infantum.

Chickenpox

  • Caused by Varicella-Zoster virus (aka, Human Herpes Virus-3)
  • Average incubation period is 16 days.
  • Often affects children younger than 5.
  • Prior to rash, patients may experience fever, malaise, sore throat, and low appetite.
  • Rash is characterized by crops of lesions that pass through macular, vesicular, and crusted phases.
    – Lesions usually first appear on the head/neck, and spread to the rest of the body.
  • Clinical correlation: Shingles is an illness that occurs in adults upon reactivation of the Varicella-Zoster Virus; the reactivated virus is called Herpes-Zoster Virus.
    – Whereas the chickenpox rash is often itchy, the shingles rash can be very painful. Vaccination against Varicella-Zoster virus also prevents shingles.

Measles (aka, rubeola)

  • Caused by the Measles virus.
  • Average incubation period is 14 days.
  • Prior to rash, patients often experience Fever and the “Three C’s”Cough, Coryza (runny nose), and Conjunctivitis.
  • These symptoms are followed by a *maculopapular rash that begins on the face and neck and spreads.
  • Before the body rash, many patients also develop Koplik spots, which are spots along the palate and internal buccal surfaces (these spots are sometimes calked Koplik’s sign).
  • Serious complications from measles virus infection include potentially fatal pneumonia and encephalitis; vaccination helps to prevent these and other complications.

Rubella (aka, German measles)

  • Caused by Rubella virus.
  • Average incubation period is 14 days.
  • Rubella is characterized by the acute onset of a pink maculopapular rash that begins on the face and spreads.
    – The rash lasts about 3 days, so Rubella is sometimes called “3-Day measles” – careful not to confuse this with Roseola infantum, which is sometimes called “3-Day Fever.”
  • Some patients also have swollen lymph nodes in the neck area; systemic symptoms, such as headache, are mild if present.
  • Congenital rubella, which is contracted during fetal development, is associated with severe birth defects; this form of rubella can also be prevented by the rubella vaccine.

Davenport Diagram

DAVENPORT DIAGRAMS:

  • Davenport diagrams are graphic displays of acid-base states.
  • They illustrate the dynamic relationships between arterial blood pH, bicarbonate and non-bicarbonate buffers, and the partial pressure of carbon dioxide.
  • An isopleth represents all possible combinations of bicarbonate and pH values at a given carbon dioxide partial pressure.

4 simple acid-base disorders prior to compensation

Graph Features:

  • The x-axis tracks pH; the healthy homeostatic arterial blood value = 7.4
  • Values less than this reflect acidosis; values higher reflect alkalosis.
  • The y-axis tracks bicarbonate concentration; the healthy homeostatic value 24 millimolar.
  • Recall that, as bicarbonate concentration increases, pH becomes more alkaline.
  • Isopleth for a partial pressure of carbon dioxide of 40 mmHg.
  • A straight line to represent the combination of all non-bicarbonate buffer titration curves.

Disorders that cause the blood to become more acidic.

  • Metabolic acidosis occurs when the reduction in bicarbonate concentration lowers the pH.
    • Notice that, because this is a non-respiratory disorder, PaCO2 is unaffected.
  • Respiratory acidosis occurs when the lungs retain excess carbon dioxide, so the partial pressure of carbon dioxide is elevated above normal, which lowers the pH. – Recall that respiratory acidosis produces an elevated bicarbonate concentration, which is reflected in our graph.

Disorders that cause the blood to become alkalotic (aka, basic).

  • Metabolic alkalosis occurs when bicarbonate concentration is elevated.
    • As in metabolic acidosis, the PaCO2 remains on the 40 mmHg isopleth.
  • Respiratory alkalosis occurs when the lungs release too much carbon dioxide
    • Lowers the PaCO2 and increases pH.

Compensatory Mechanisms

  • The lungs and kidneys respond to acid-base disorders via compensatory mechanisms that bring pH back to normal.

When metabolic acidosis triggers release of carbon dioxide from the lungs, PaCO2 falls and pH increases.

  • Thus, our point of interest lies lower and to the right than on our original graph.
    • Shaded area represents all possible outcomes of partial compensation for metabolic acidosis; the extent of the original disturbance and the magnitude of compensation determine the specific blood outcome.

When respiratory acidosis triggers increased renal excretion of hydrogen ions and conservation of bicarbonate, pH increases.

  • The partial pressure of carbon dioxide remains elevated until the source of the disorder is treated, because the lungs are unable to expel CO2.

When metabolic alkalosis triggers respiratory and renal mechanisms to conserve hydrogen ions, pH lowers.

  • However, because the respiratory component of compensation requires conservation of carbon dioxide, its partial pressure remains elevated.

When respiratory alkalosis triggers renal mechanisms that conserve hydrogen ions, pH lowers.

  • But, until the source of the disorder is treated, the partial pressure of carbon dioxide will remain below 40 mmHg.

Perfect Compensation – Blood pH returned to 7.4

  • The blood profile end-states reflect both the original disorders and the compensatory mechanisms.

If the original disorder was metabolic acidosis or respiratory alkalosis, both the bicarbonate concentration and the partial pressure of carbon are reduced (isohydric hypocapnia).

  • In the case of metabolic acidosis, this new state is accounted for by:
    • The cause of the disorder, which was a low concentration of bicarbonate
      relative to hydrogen ions.
    • The respiratory component of compensation, which required increased release
      of carbon dioxide.
  • In the case of respiratory alkalosis, this new state is accounted for by:
    • The cause of the disorder, which was the excessive release of carbon dioxide, and,
    • Renal compensatory mechanisms that excreted bicarbonate.

If the original disorder was respiratory acidosis or metabolic alkalosis, both the bicarbonate concentration and the partial pressure of carbon dioxide are elevated above normal (isohydric hypercapnia).

  • In the case of respiratory acidosis, this is state is accounted for by:
    • The cause of the disorder, which was over-retention of carbon dioxide, and,
    • Renal compensatory mechanisms that conserved bicarbonate.
  • In the case of metabolic alkalosis, this state is accounted for by:
    • The cause of the disorder, which was an increased bicarbonate to hydrogen ion ratio
    • The respiratory component of compensation, which required increased carbon
      dioxide retention in the lungs.

Compound Disturbances:

  • If both metabolic and respiratory acidosis are in play, pH is reduced more so than if just one disorder was influencing pH; the shaded area shows the range of possible values that could result.
  • When alkalosis results from both metabolic and respiratory origins, pH is elevated more so than if only one disorder was present.
    • Be aware that while this information can tell us if there are one or two sources of the pH disturbance, it cannot tell us which preceded the other.

Congenital Intestinal Defects

MIDGUT MALFORMATIONS

  • Rotation defects
  • Omphalocele
  • Meckel’s diverticulum
Recall that, typically, the primary intestinal loop undergoes 270 degrees counterclockwise rotation as it elongates; in the final position, the large intestine “frames” the small intestine.

Rotation Defects

  • Non-rotation
    • When rotation does not occur, the small intestine lies to the right of the large intestine (thus, it this defect is sometimes referred to as “left-sided colon”).
  • Reversed rotation
    • When rotation occurs clockwise; in this case, the duodenum will pass ventral to the transverse colon, instead of dorsal to it.
  • Mixed rotation
    • When rotation of the cranial and caudal intestinal segments is not coordinated: only the cranial end undergoes the first rotation, and only the caudal end undergoes the second. The cecum lies at the midline, just inferior to the pyloric region of
      the stomach. Because the mesentery is pulled with the intestine as it rotates, mixed rotation can resort in volvulus, aka, torsion, of the mesentery around the superior mesenteric artery. Bands of mesentery can constrict and obstruct the digestive tract; the duodenum is particularly susceptible to entrapment by the mesentery of the cecum.

Omphalocele

  • Occurs when the abdominal viscera protrude through the umbilical ring
    • The viscera is covered in a vascular membrane, which is susceptible to rupture (not to be confused with gastroschisis, in which the viscera protrude from the anterior body wall but are not covered by a membrane).
    • Omphalocele is often present in conjunction with other abnormalities, and is thought to occur as result of failure to fully retract during midgut rotation, lateral body folding failures, or failure of connective tissues in the abdominal wall.

Meckel’s diverticulum

  • Present when the vitelline duct fails to fully regress.
    • Its location and length are variable, and, in many cases, is asymptomatic. However, if the diverticulum contains pancreatic or gastric tissues, bleeding ulcers can form.

HINDGUT MALFORMATIONS

  • Fistulas
  • Imperforate anus

Fistulas

  • Rectourethral fistulas occur when the urinary and digestive tracts are connected.
    • Thus, both urine and feces are directed through the urethra, and surgery is required.
  • Rectovaginal fistulas are characterized by a connection between the vagina and rectum.
    • The connection between the rectum and vagina channels rectal contents to the vagina; surgery is required to form a separate outlet for feces.
      Imperforate anus

Presents in various permutations; corrective surgeries are necessary to treat imperforate anus, which is often accompanied by fistula.

Agenesis

  • Characterized by the formation of a blindly ending anorectal canal.

Anal atresia

  • Occurs when the anal membrane is abnormally thick, and prevents the anus from opening to the external environment.

Viral Enteric & Hepatic Infections

  • The enteric viruses we’ll learn about are naked capsids that can withstand harsh stomach acids.
  • When symptomatic, illness is characterized by diarrhea and vomiting.
  • Outcomes are often worse for children and infants, due to malnutrition and dehydration stemming from fluid and electrolyte loss.
  • The causative viruses are transmitted via the fecal/oral route.
  • Hepatic viruses cause tissue damage and trigger inflammatory responses that produce the symptoms of infection.

Enteric Viruses

  • Cause acute gastroenteritis and are typically ingested via contaminated food and water.
    – Vomiting and diarrhea.
    – Other symptoms include possible fever, nausea, abdominal pain or cramping, and myalgia and malaise.
    – Rehydration and electrolyte therapy are common treatments.
  • Key viral causes of gastroenteritis:
    –  Norovirus is a leading cause of gastroenteritis in all age groups in the United States; outbreaks have been associated with contaminated shellfish.
    –  Adenovirus accounts for approximately 15% of hospitalized gastroenteritis cases, especially in infants. Recall that adenovirus also causes respiratory and ocular infections.
    – Astrovirus causes mild, watery diarrhea, most commonly in children.
    However, extra-intestinal infections can occur in immune-compromised patients; some viral genotypes, for example, have been associated with central nervous system infections.
    – Rotavirus is the leading cause of severe diarrhea worldwide in children under five years old; in premature neonates, rotavirus can manifest as necrotizing enterocolitis or hemorrhagic gastroenteritis.
    Because of the high morbidity and mortality associated with rotavirus, vaccination is recommended for all infants.
  • In immune compromised patients, particularly AIDS patients and transplant recipients, cytomegalovirus (CMV) and Epstein-Barr Virus are associated with gastroenteritis.
  • For a list of bacterial pathogens that induce enteric illnesses, see here.

Hepatic Viruses: Hepatitis Viruses A, B, C, D, and E,

  • Hepatitis is characterized by inflammation of the liver.
    – Acute hepatitis = Inflammation that lasts less than 6 months
    – Chronic hepatitis = Inflammation that lasts 6 months or longer
    – In some cases, hepatitis can lead to fulminant liver failure; write that this is characterized by rapid, acute livery injury with hepatic encephalopathy.
  • Vaccine availability varies for the hepatitis viruses, and there is no vaccine for Hepatitis C virus due to its heterogeneous nature.

Acute hepatitis

  • Hepatitis A, B, C, D, and E can cause acute hepatitis.
  • Symptoms include: Jaundice, nausea and vomiting, abdominal pain, dark urine, and joint pain, as well as low or no appetite and fatigue.
    – Liver failure is possible with acute hepatitis, but rare.
  • General features of acute hepatitis histopathology:
    – Ballooning degeneration: hepatocytes are unusually large, with a “whispy” look
    – Spotty necrosis throughout the liver tissue
    – Mononuclear cell infiltrate
    – Councilman bodies, which are shrunken, acidophilic cells.
  • Hepatitis A and E only cause acute hepatitis, not chronic.
    – Both viruses are transmitted via the fecal-oral route, often via contaminated water.
    – No carrier state for these Hepatitis viruses.
    – Both typically cause mild and self-limiting acute hepatitis; fulminant liver failure is possible but rare.
    – An important exception is that Hepatitis E infection has high mortality rates in pregnant women, especially during the third trimester.

Chronic hepatitis

  • Caused by Hepatitis BD, and C.
  • Chronic infections can lead to scarring, cirrhosis, and cancer.
    – Smoking, alcohol use, age, sex, and population seem to increase the risk of disease progression.
  • Hepatitis viruses B, D, and C are transmitted via body fluids
    – Carrier states exist
    – Hepatitis B can be transmitted from mother to neonate during childbirth.
    – Hepatitis C often produces extra-hepatic effects, including cryoglobulinemia vasculitis and B-cell non-Hodgkin’s lymphoma, and other immune mediated and inflammation mediated diseases.
    – Hepatitis D is often called the “Delta agent”; though infection with Hepatitis D, alone, does not produce illness, when combined with Hepatitis B, it makes infection worseand increases the risk of Fulminant liver failure.
  • Hallmarks of Hepatitis B and C histopathology:
    – Hepatitis B often produces “ground glass” hepatocytes; the tiny grains in the cytoplasm are from viral protein accumulation.
    – Hepatitis C infection is characterized by lymphocyte aggregates and follicles, especially around the portal tracts;
    bile ducts are often damaged, and, steatosis (also called fatty change) can also occur.

The Pharyngeal Arches – Part 1

  • There are 5 pharyngeal arches, numbered 1 – 4 and then 6.

(There is NO 5th pharyngeal arch.)

  • They comprise:
    • Aortic arches, the arterial connections between the ventral and dorsal aortae.
    • Skeletal structures (derived from neural crest cells).
    • Muscle (derived from mesoderm).
    • Cranial nerves (derived from neural crest cells).

THE PHARYNGEAL ARCHES AND THE NEURAL CREST CELL MIGRATIONS TO FORM CNS 5, 7, 9, AND 10

We draw the differentiated neural tube from cranial to caudal:

  • Telencephalon
  • Diencephalon
  • Mesencephalon
  • Metencephalon
  • Myelencephalon

And we include the caudal neural tube

  • The notochord induces the overlying ectoderm to differentiate into the neural tube.
  • There are 5 pharyngeal arches, from cranial to caudal: 1, 2, 3, 4, (skip 5) and then 6 [No 5th Pharyngeal Arch exists!]

Neural crest cells migrate into the pharyngeal arches and to form the pharyngeal arch cranial nerves.

  • CN 5 (the trigeminal nerve) migrates into arch 1
  • CN 7 (the facial nerve) migrates into arch 2
  • CN 9 (the glossopharyngeal nerve) migrates into arch 3
  • CN 10 (the vagus nerve) migrates into arches 4 and 6 – the superior laryngeal branch lies within the 4th pharyngeal arch and the recurrent laryngeal branch lies within the 6th pharyngeal arch.

In addition to the cranial nerves being a part of this migration, so are the skeletal elements.

  • The mandibular prominence forms pharyngeal arch 1 (if we know CN 5’s role in mastication, this will help us remember the association between this arch and nerve).
  • Although the maxillary prominence is sometimes listed as a portion of pharyngeal arch 1, indicate that it actually lies rostral to the 1st arch.

Key placodes (which are areas of thickened surface ectoderm) derive CNs 1, 2, and 8 (the solely sensory set of CNs), from cranial to caudal.

  • At the nasal prominence, lies the olfactory placode, which derives the olfactory epithelium and olfactory nerve (CN 1).
  • The optic placode forms the optic nerve (CN 2); it originates from the diencephalon.
  • The otic placode forms the vestibulocochlear nerve (CN 8); it originates from the hindbrain.

THE PHARNGYEAL APPARATUS (AKA THE PHARYNGEAL REGION): THE PHARYNGEAL POUCHES AND AORTIC ARCHES.

Whereas the neural tube lies dorsal to the notochord, the structures we’ll focus on here (the vasculature and pharyngeal apparatus) lie ventral to it.

  • The long endodermal tube follows the cephalic bend ventral to the notochord.
    • Cranially, lies the pharynx.
    • Caudally, label the esophagus.
  • The trachea branches from the endodermal tube anterior to the esophagus.

4 pharyngeal pouches lie along the endoderm

We specify that the 1st pharyngeal pouch lies posterior to the 1st pharyngeal arch.
  • The pouches are outpouchings of endoderm that fill the pharyngeal grooves; we’ll understand this anatomy better in part 2 of our diagram in which we draw the pharyngeal apparatus in coronal view.

Arterial vasculature

  • Each pharyngeal arch has an aortic arch that runs within it.
  • From the heart emanates the truncus arteriosus, aortic sac, and the ventral aorta.
  • The dorsal aorta bifurcates to become the bilateral internal carotid arteries, cranially – they form the primary supply of blood to the brain (the anterior 2/3rds of the brain’s vascular supply). For reference, the posterior blood supply to the brain comes from the basilar artery, which is supplied by the vertebral arteries.
  • Connect the ventral and dorsal aortae with the aortic arches that pass in between the pharyngeal pouches and specify the 1st aortic arch (these are sometimes referred to simply as the arch arteries) – they connect the dorsal and ventral aortae.

THE PITUITARY GLAND

  • Rathke’s pouch is an ectodermal placode along the roof of the stomodeum (the site of the future mouth – the cranial opening of the pharyngeal apparatus). Rathke’s pouch stretches towards the floor of the 3rd ventricle (the infundibulum). Later, it disconnects from the stomodeum and its stalk regresses: ultimately, forming the anterior pituitary gland. And the infundibulum descends and develops into the posterior pituitary gland.
    • Clinical Correlation: Craniopharyngioma
These fascinating embryological migrations help us to remember that the pituitary gland is acutely in touch with the external environment and works to keep our body in physiological homeostasis.

THE THYROID GLAND

  • The thyroid primordium lies in between the 1st and 2nd pharyngeal pouches, along the ventral surface of the pharyngeal apparatus, draw. It forms at the apex (the ventral tip) of the foramen cecum.
  • The thyroid primordium develops into the thyroid gland, which descends within the thyroglossal duct (which quickly breaks down) and then migrates beneath the thyroid cartilage to its ultimate anatomical site: beneath the cricoid cartilage.

Clinical Correlation –

The cricoid cartilage is an important anatomical landmark when palpating for a thyroid goiter!

Embryonic Folding

The trilaminar embryo at approximately day 21

Using standard embryological convention:

  • The ectoderm in blue (within the amniotic cavity)
  • The endoderm in yellow (within the yolk sac)
  • Intraembryonic mesoderm lies in between them.
  • Extraembryonic mesoderm surrounds the embryo.

Day 23

  • The extraembryonic mesoderm forms a mushroom shape (forming what appears to be a cap and the beginning of a stalk)
  • The ectoderm-lined floor of the amniotic cavity curls under at its edges the endoderm-lined roof of the yolk sac, also tucks under.
  • Accordingly, so does the intraembryonic mesoderm.

Day 26

  • The extraembryonic mesoderm further curls and the stalk (the vitelline duct) narrows.
  • The curling of the amniotic cavity accentuates and so does the yolk sac and the intraembryonic mesoderm.

THE TRILAMINAR GERM DISC STRUCTURES AT DAYS 21, 23, AND 26

Day 21

from top to bottom

  • The trilaminar germ disc comprises ectoderm, mesoderm (which is intraembryonic), and endoderm.
  • Within the mesoderm, lies the the ectoderm-derived neural tube, notochord, bilateral somites, and neural crest.
  • There is folding of the neural tube.
    • the neural folds abut centrally, first, but remain open at their ends anteriorly and posteriorly.
    • the neural groove lies deep within the neural tube.
    • the neural crests form at the tips of the neural folds.

Day 23

  • The neural crest cells are now making their migrations.
  • Neural tube folding:
    • The neural tube is now folded a long distance along its center but remains open at the anterior and posterior neuropores.
    • We see the somites, centrally, where the neural folds abut; they generate bumps that appear on the surface of the overlying neural tube.

Day 26

  • The somites (the paraxial mesoderm) differentiate into the central musculoskeletal elements – (from medial to lateral): sclerotome (which forms bone), myotome (which forms muscle), and dermatome (which forms skin).

EMBRYONIC FOLDING WITH THE DEVELOPMENT OF THE KEY STRUCTURES OF THE TRILAMINAR GERM DISC

The trilaminar embryo at approximately day 21

Using standard embryological convention:

  • The ectoderm in blue (within the amniotic cavity)
  • The endoderm in yellow (within the yolk sac)
  • Intraembryonic mesoderm lies in between them.
  • Extraembryonic mesoderm surrounds the embryo.
  • The connecting stalk connects the embryo to the uterus.
  • The embryo lies within the chorionic cavity, which, itself, is lined with extraembryonic mesoderm.
  • The allantois is the tip of the posterior endoderm that extends into the connecting stalk – a hindgut diverticulum.

Day 23

  • The extraembryonic mesoderm forms a mushroom shape (forming what appears to be a cap and the beginning of a stalk)
  • The ectoderm-lined floor of the amniotic cavity curls under at its edges the endoderm-lined roof of the yolk sac, also tucks under, accordingly, so does the intraembryonic mesoderm.
  • The connecting stalk is tucked under the endo- and ectodermal folds.
  • The neural tube is now folded a long distance along its center but remains open at the anterior and posterior neuropores.

Day 26

  • The extraembryonic mesoderm further curls and the stalk (the vitelline duct) narrows.
  • The curling of the amniotic cavity accentuates and so does the yolk sac and the intraembryonic mesoderm.
  • There is further folding of the connecting stalk and outpouching of the endodermal allantois.
  • There’s further the growth of the neural tube, which is fully closed (anterior and posterior neuropores have closed).
  • The gut structures endoderm forms are visible: from anterior to posterior – the foregut, midgut (which attaches to the yolk sac via the vitelline duct), and the hindgut.

Neurulation

Definiton

  • The process of neurulation involves the formation of the neural plate and the folding of the neural plate into the neural tube.

Key Points

  • The notochord induces the overlying ectoderm to develop into the neural plate.
  • The neural plate folds into the neural tube and as it closes, the neural crests are pinched off.
  • The neural tube derives the central nervous system (the brain and spinal cord).
  • The neural crest cells derive the peripheral nervous system (eg, ganglion cells and Schwann cells) and also select other cell types (eg, melaoncytes).

THE DEVELOPING EMBRYO

Trilaminar germ disc

Three layers of the trilaminar germ disc.

  • Ectoderm (and amniotic cavity)
  • Mesoderm
  • Endoderm (and yolk sac)

THE NOTOCHORD

The prochordal knot

  • A strand of cells that extends toward the cranial end of the prochordal knot.
    • The prochordal knot lies within the mesoderm (in between the ectoderm and endoderm).

ASSOCIATED EMBRYONIC STRUCTURES

Key associated embryonic structures:

  • The primitive streak exists within the ectodermal layer of the germ disc; it dimples along the embryonic disc.
  • The primitive node (aka primitive knot, Hensen’s node) lies at the cranial end of the primitive streak.
  • The prochordal knot lies farther cranially.

NOTOCHORD DEVELOPMENT

  • The notochord develops cranially, (towards the head of the embryo) and because it is blocked at the prochordal plate, it also develops caudally (towards the tail of the embryo) as the primitive streak regresses. There are multiple stages of notochord development, which we omit, here, for simplicity.

Key notochord actions:

  • Forms the embryonic central axis,
  • Induces neural plate formation,
  • Establishes the central column of the spine and then degenerates to become the nucleus pulposus of the intervertebral discs.

DAY 17 OF EMBRYOGENESIS

  • Early regression of the primitive streak.
  • Development of the neural plate.
  • The notochord lies within the mesoderm (it induces neural plate formation).

DAY 18 OF EMBRYOGENESIS

  • The primitive streak has regressed.
  • The neural plate invaginates to form the neural groove (the dip, centrally) and the neural folds (the peaks, laterally). The neural crests lie at the tips of the neural folds.
  • Within the mesoderm, somites develop.

Somite differentiation

  • Sclerotome (which derives bone and cartilage),
  • Dermatome (which derives dermis),
  • Myotome (which derives skeletal muscle).

DAY 21 OF EMBRYOGENESIS.

  • The primitive streak has nearly completely regressed and the neural groove starts to fully fold to form the neural tube, which enters the mesoderm.
  • It closes off in the center first, with the cranial and caudal ends still open at this point, and resides within the mesoderm.
  • The neural crest cells have pinched off and reside in the ectoderm layer.

DAYS 23 – 26 OF EMBRYOGENESIS

  • The anterior (cranial) neuropore closes at approximately Day 24.
  • The posterior (caudal) neuropore closes at approximately Day 26.
  • The somites form ridges underneath the ectoderm.
  • The neural crests migrate to within the mesoderm.

CONGENITAL NEURO EMBRYOLOGICAL DISORDERS

  • Chordoma
  • Chiari Malformation
  • Dandy Walker Malformation
  • Encephalocele
  • Holoprosencephaly
  • Lissencephaly
  • Schizencephaly
  • Septo-Optic Dysplasia
  • Zellweger Syndrome

Gastrulation

GASTRULATION

The embryonic disc develops from bilaminar (2 layers) to trilaminar (3 layers).

The bilaminar disc comprises epiblast + hypoblast.

The trilaminar disc comprises ectoderm, mesoderm, endoderm.

All of which derives from the epiblast (none from the hypoblast).

BLASTOCYST FORMATION

The blastocyst is a circular cyst; it’s divisions are:

  • Trophoblast: the outer cell mass.
  • Embryoblast: the inner cell mass.

The blastocyst resides within the uterine cavity and eventually invades the uterus.

The uterine walls, from inside to outside, are:

  • Endometrium
  • Myometrium
  • Perimetrium

TROPHOBLAST DIVISION

Trophoblast divides into:

  • Cytotrophoblast, the inner cell line, which maintains a similar shape as the trophoblast.
  • Syncytiotrophoblast, the external cell line, which invades the uterine wall to lay the foundation of the placenta.

Within the cytotrophoblast, the embryoblast transforms into:

  • The epiblast (which are columnar cells) – the original mass of inner cells
  • The hypoblast (which are small cuboidal cells) – a new layer of cells underneath the epiblast.

The bilaminar germ disc exists where the epiblast and hypoblast meet.

At this stage, the syncytiotrophoblast invades into the uterine wall.

EPIBLAST DIVISON

The epiblast generates cells that become:

(1) Ectoderm

  • Amniotic cavity fills the cavity internal to the ectoderm.
    (2) Endoderm
  • Yolk sac fills the cavity internal to the endoderm.
    (3) Mesoderm

GASTRULATION

Ectoderm forms the primitive streak: a dimpling at the germ disc – the site of gastrulation.

  • Gastrulation is a process of invagination, wherein ectodermal cells pass from the ectodermal surface to the primitive streak. Mesodermal cells spread out between the ectoderm and endoderm and also surround these cell lines.

The germ disc is now trilaminar.

In addition to the mesoderm mentioned previously, there also exists an additional mesoderm layer: the extraembryonic mesoderm just internal to the cytotrophoblast.

GERM LAYER DERIVATIVES

The key germ layer derivatives (note that these are numerous and we only list the highlights):

Ectoderm

  • Skin + derivatives (hair, nails, etc…)
  • Adrenal medulla
  • Nervous tissue
  • Sense organs

Mesoderm

  • Musculoskeletal (including heart muscle)
  • Adrenal cortex
  • Testes + ovaries
  • Kidneys + ureters

Endoderm

  • Epithelial lining of: GI, Respiratory, Urinary, Reproductive systems