Orofacial Embryology Flashcards

1
Q

branchial refers to…

A

gills- eventually the precursor for neck and lower 2/3 of face like mouth ear and neck

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2
Q

4 components of pharyngeal apparatus

A
  1. arches- bulge outward from neck region
  2. cleft/groove- external invagination b/w arches
  3. pouch- internal invagination b/w arches
  4. membrane- tissue separating cleft and pouch
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3
Q

when and where do the arches arise

A

week 4, cranial to caudal
1,2,3,4,6

give rise to lower 2/3 of face, oral cavity, ear, neck

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4
Q

3 layers of arches

A
  1. external- from ectoderm
  2. filling/core- from mesoderm and neural crest, neural crest must migrate into arches for proper skeletal tissue formation
  3. internal- from endoderm, forms GI tract lining
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5
Q

innervation of the 5 arches

A
1=5
2=7
3=9
4=10
6=10
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6
Q

5 areas that give rise to the face

A

frontonasal process and 2 maxillary processes and 2 mandibular processes

meet at the mouth eventually

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7
Q

arch 1 gives rise to… (bones)

A

lower 2/3 of face- skin, muscle, bone

bone:
- maxillary process, forms that bone, palate, zygomatic, squamous temporal
- lower jaw, mandibular process: mandible, sphenoid spine, malleus, incus
- sphenomandibular ligament, anterior ligament of malleus

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8
Q

what is meckel cartilage

A

origin of mandibular process of arch 1

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9
Q

arch 1 muscle derivatives

A

muscle: all innervated by CN5, muscles of mastication

- mylohyoid, masseter, temporalis, anterior digastric, tensor tympani, tensor veli palatini

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10
Q

formation of lower lip and jaw

A

arch 1 mandibular processes fusing at midline, rare anomalies

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11
Q

formation of upper lip and jaw

A

more common- 3 areas are fusing

2 maxillary processes fusing w/ medial nasal process (philtrum)

anomolies more common, cleft lip and palate

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12
Q

difference b/w cleft lip and palate, incomplete vs complete

A

cleft lip: clefting anterior to incisive foramen (meeting of processes)

cleft palate: clefting posteriror to foramen

incomplete- partial lack of fusion
can be unilateral or bilateral

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13
Q

skeletal derivatives of arch 2

A

aka hyoid arch

starts w/ reichert cartilage- forms lesser horn of hyoid, stylohyoid ligament, styloid process, stapes

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14
Q

muscles from arch 2

A

all from CN7

muscles of facial expression- posterior digastric, stylohyoid, stapedius

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15
Q

skeletal derivatives of arch 3

A

starts w/ cartilage, forms body and greater horn of hyoid

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16
Q

muscles from arch 3

A

from CN 9

stylopharyngeus

17
Q

skeletal derivative of arch 4,6

A

from cartilage- laryngeal cartilage (cricoid, thyroid, arytenoids, etc)

18
Q

muscles from arch 4,6

A

all from CN10

arch 4: pharyngeal constrictors, cricothyroid, levator veli palatini

arch 6: all laryngeal except cricothyroid

19
Q

describe phayngeal arch vasculature and what they become

A

each arch as 1 artery called aortic arch

1,2,5 disappear

3=common carotid
4= right subclavian and arch of aorta
6= pulm arteries

20
Q

arch contribution to the tongue

A

arch 1: anterior 2/3 (CN5 for somatic, 7 for taste)

arch 3: posterior 1/3 (CN9 for somatic and taste)

arch 4: base and epiglottis (CN 10 for both)

think cranial to caudal

21
Q

what happens to branchial clefts

A

2-4 disappear as arch 2 covers them up, temporarily creates cervical sinus

cleft 1 becomes external acoustic meatus- from ectoderm

22
Q

what is a branchial cleft cyst

A

persistent cervical vesicle/sinus

along anterior border of SCM muscle

23
Q

derivatives of 4 pouches

A

note these are internal, endoderm

  1. eustachian tube
  2. palatine tonsil
  3. thymus, inferior parathyroids
  4. superior parathyroids
24
Q

etiology of diGeorge syndrome

A

abnormal development of pouch 3 and 4- lack of thymus and parathyroids causes immune deficiency, hypocalcemia, facial/palate problems

25
Q

derivatives of branchial membranes

A

2-4 disappear under arch 2 overgrowth

1 becomes tympanic membrane (pouch 1 was eustachian tube)

26
Q

describe formation of ear, preceding structures (4)

A

arch 1,2: auricle

cleft 1: external accoustic meatus

membrane 1: tympanic membrane

pouch 1: eustachian tube

27
Q

list some facial characteristis of fetal alcohol syndrome

A

small head, low nose, thin upper lip, small eye openings

some due to neural crest cell injury or impaired migration