1 - Embryology Flashcards

1
Q

Describe the process of neurulation.

A

1) Beginning of 3rd wk: ectoderm overlying notochord thickens to form neural plate; lateral edges form neural folds; neural groove forms between folds; folds + groove = neuroectoderm
2) folds join midline and form neural tube; cells from the apices of the folds migrate to form neural crest
3) tube is first formed at the occipital region and then proceeds cranially and caudally-> cranial @25th; caudal @28th
4) The rostral portion enlarges to become the brain, the caudal end thins to become the cord

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2
Q

What happens if the neural tube fails to close?

A

Neural Tube Defects
Caudal:
-Spina bifida occulta: vertebral arch is defective, skin may be covered by tuft of hair
-Spina bifida cystica:
w/ meningocele -> meninges protrude through vertebral arch and skin
w/ meningomyelocele -> both meninges and neural tissue protrude through vertebral arch and skin
-Rachischisis: neural folds fail to elevate or close, forming an exposed flattened mass of neural tissue
Cranial NTD:
-Meningocele: only meninges bulge through an occipital bone defect
-Meningoencephalocele: meninges and brain tissue bulge through an occipital bone defect
-Meningohydrencephalocele: meninges, brain tissue and part of the ventricular system bulge through an occipital bone defect
-Anencephaly: failure of anterior neuropore closure with most of brian and skull roof absent

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3
Q

What type of cells develop from neural crest cells?

A
  • pigment cells
  • dorsal root ganglia, cranial nerve ganglia
  • schwann cells and satellite cells
  • sympathetic and parasympathetic ganglia
  • adrenal medulla chromaffin cells
  • c-cells of thyroid gland
  • dentin
  • facial skeleton
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4
Q

Describe the histogenesis of neurons.

A

1) Neuroepithelial cells comprise ventricular zone of the neural tube
2) These develop into primitive neuroblasts after tube closes
3) These migrate to Mantle Layer surrounding ventricular layer where they differentiate into neurons
4) This continues until ~6mo gestation, and ~1yr postnatal in the cerebellum
5) Mature neurons migrate within the brain via radial glial cells
6) Axons from the maturing neurons form a Marginal Layer around Mantle layer

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5
Q

Describe the histogenesis of glial cells.

A

1) Neuroepithelial cells comprise the ventricular zone on the inside of the neural tube
2) After neuron genesis is complete, the neuroepithelial cells differentiate into glioblasts
3) These in turn differentiate into astrocytes and oligodendrocytes
4) Once glial cells are formed, the remaining neuroepithelium develop into ependymal cells, which will line the ventricles of the adult brain
5) Microglia are thought to develop from mononuclear hematogenesis in the bone marrow and migrate to the brain during development

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6
Q

What are Alar and Basal Plates? What do they develop into?

A

The mantle layer of the spinal cord thickens and is divided by the development of the Sulcus limitans; creating the Alar and Basal Plates (Dorsal and Ventral horns).
The mantle layer becomes the white matter of the CNS and the center the ventricle of the adult brian.

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7
Q

Describe the development of the brainstem.

A
  • Develops similar to the spinal cord with alar(dorsal) and basal(ventral) plates developing.
  • In the region of the pons/medulla, the central canal opens to form the 4th ventricle
  • This opening displaces the plates so that the alar plates are now lateral and the basal plates medial to the sulcus limitans
  • This arrangement is seen in the pyramids and olives of the adult medulla which retain their motor and sensory nuclei
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8
Q

Describe the development of the cerebellum.

A
  • metencephalon and dorsolateral portion of alar plate expand to form Rhombic Lips
  • these grow into 4th ventricle and are separated by a thin Roof Plate
  • the rhombic lips overgrow the roof plate and meet to form the respective cerebellar hemispheres
  • the roof plate represents the Vermis of the adult cerebellum
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9
Q

What is the Arnold-Chiari malformation?

A

Congenital hypoplasia of the posterior cranial fossa does not allow adequate room for the growing cerebellum. This causes “herniation” of the tonsillar cerebellum through the foramen magma. However, the foramen typically expands during development allow with herniation, therefore it is frequently asymptomatic or presents late with only mild symptoms. Tx with surgery.

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10
Q

Describe the development of the telencephalon.

A

1) Rostral proencephalon develops two hollow bulges that develop into the telencephalic vesicle/cerebral hemispheres
2) The cavities of the vesicles will become the lateral ventricles
3) The vesicles continue to grow and “wrap” around the diencephalon in a C-shape that is seen in several adult brain structures
4) The major commissures (corpus colostrum, anterior and posterior commissure) develop from the region of the lamina terminalis
5) The cortex develops as maturing neurons travel outward in Radial or Tangential Migration guided by Radial Glial Cells
6) The migration causes the cortex to go from smooth (lissencephalic) to pitted by sulci to increase surface area -> continues into 5-7th prenatal month

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11
Q

What are the cranial nerves associated with each of the pharygeal arches?

A
  • 1st Arch -> CN V3 (mandibular division of trigeminal)
  • 2nd Arch -> CN VII (facial)
  • 3rd Arch -> CN IX (glossopharyngeal)
  • 4th Arch -> CN X (Vagus)
  • 6th Arch -> CN X (recurrent laryngeal nerve)
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12
Q

What are the adult derivatives of the aortic arches?

A
  • 1st and 2nd Arches degenerate.
  • 3rd Arch develops into the Common carotids and join with the part of the Dorsal Artery to form the Internal and External Carotids
  • 4th Arch forms the subclavian on the right and the aortic arch on the left
  • 5th (doesn’t exist)
  • 6th Arch forms the pulmonary arteries
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13
Q

What are the muscular derivatives of the pharyngeal arches?

A

1) MM-MATT: Muscle of Mastication, Mylohyoid, Anterior belly of Digastric, Tensor Tympani, Tensor Veli Palatini
2) FESSP: Fascial Expression, Stapedius, Sylohyoid, Posterior belly of Digastric
3) Stylopharyngeus
4) Palate Muscles(NOT tensor veli palatini), pharynx muscles(NOT stylopharyngeus), cricothyroid
6) Layngeal muscles (not cricothyroid)

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14
Q

What are the skeletal derivatives of the pharyngeal arches?

A

1) Maxilla, mandible, malleus, incus, squamous temporal, sphenomandibular ligament
2) Stapes, styloid, hyoid (top), stylohyoid ligament
3) hyoid (lower)
4) Laryngeal cartilage
6) Laryngeal cartilage

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15
Q

What is the embryonic origin of the eardrum?

A
  • The external auditory canal is formed from the 1st pharyngeal cleft
  • the tympanic membrane (eardrum) is formed from the layering of the ectoderm and endoderm (and some mesoderm) from the 1st pharyngeal cleft
  • the pharyngotympanic membrane is formed from the outgrowth of the 1st/2nd pharyngeal pouches
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16
Q

What are the adult derivatives of the pharyngeal pouches?

A

1) middle ear cavity and auditory tube
2) Tonsillar crypts
3) Inferior parathyroids, thymus
4) Superior parathyroids
5) C cells (from neural crest) of the thyroid gland

17
Q

Describe the development of the floor of the pharynx.

A
  • in the area of the 1st pharyngeal arch, there develop two lateral swellings separated by a midline tubercle -> become anterior 2/3 of tongue
  • the copula (from 2,3 and 4th arches) will swell and become the posterior 1/3 of the tongue
  • occipital somites will migrate to the tongue and give rise to the muscles of the tongue and carry CN XII with them
  • between the 1st and 2nd arch, a epithelial proliferation develops which will become the thyroid, which will descend to it’s final destination leaving a depression (foramen cecum) in its place
  • as it descends a thyroglossal duct develops, but subsequently degenerates
18
Q

Describe the development of the facial bones.

A

1) begins as 5 prominences: frontonasal, 2 maxillary, 2 mandibular
2) two ectodermal depressions form in the frononasal prominence (nasal placodes) with a medial and lateral nasal prominence forming around each
3) Mandibular prominences merge -> forming lower jaw
4) Medial Nasal prominences merge -> forming nasal septum, bridge and philtrum of lip
5) Maxillary prominences merge w/ Medial and Lateral Nasal prominences -> forms upper jaw and nasolacrimal ducts
6) Maxillary prominences merge with Mandibular prominences -> limits size of the oral cavity and forms cheeks

19
Q

Describe the development of the nasal cavity and palate.

A
  • The nasal placodes of the frontonasal prominence continue to indent the underlying tissue forming the nasal pits
  • the tissue between the developing nasal pits and oral cavity break down, leaving the primary palate as outgrowths of the fused Medial Nasal prominences
  • The maxillary prominences develop extensions that project into the oral cavity around the tongue
  • a downgrowth from the frontonasal prominence will become the nasal septum
  • as the tongue is lowered by the merging of the mandibular prominences, the maxillary extensions (palantine shelves), the frontonasal downgrowths (nasal septum) and the medial nasal prominence outgrouwths (primary palate) FUSE -> hard palate
20
Q

Describe the development of the following conditions:

1) cleft lip
2) cleft face
3) cleft palate
4) Treacher-Collins
5) Pierre- Robin

A

These are failures of the fusion of the prominences of the face.

1) Cleft(hare) lip: failure of fusion btwn maxillary and ipsilateral medial nasal prominence
2) Cleft face: failure of fusion btwn maxillary and both the medial and lateral nasal prominences
3) Cleft Palate: failure of fusion between palantine shelves, primary palate and nasal septum
4) Treacher Collins Syndrome: 5th Ch abnormality (tcof1)-> underdeveloped zygomatic arches and mandibular bones, downslanting palpebral fissures and malformed external ears
5) Pierre-Robin Sequence: abnormality in 1st Arch structures-> small jaw, cleft palate, posteriorly placed tongue, cheek defects, macrostomia