craniofacial development Flashcards

1
Q

prominences derived from arch 1

A

lateral nasal
medial nasal
maxillary
mandibular

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2
Q

frontonasal prominence forms?

A

forehead
bridge of nose
medial/lateral nasal prominences

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3
Q

maxillary prominence forms?

A

cheeks

lateral portion of upper lip

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4
Q

medial nasal prominence forms?

A

philtrum

crest and tip of nose

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5
Q

lateral nasal prominence forms?

A

ala of nose

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6
Q

mandibular prominence forms?

A

lower lip

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7
Q

trigeminal nerve distribution with development

A

follows derivatives of the first arch

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8
Q

embryo exposure to toxins/tetrgogens in development

A

in early stages can lead to severe deformaties/ death

later on can simply cause mild deformaties

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9
Q

neural crest cells migrating to first and second arches

A

 Neural-crest derived mesenchyme from the first and second arches migrates into the developing face
 Will give rise to bone & cartilage
 Muscles from mesoderm
 Associated with specific nerve & arteries

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10
Q

Normal Facial Development time frames

A

 Week 4
Frontonasal region
First pharyngeal arch

 5-12 Weeks
Palatogenesis-palate formation

Week 5
Cheilogenesis-nose formation

 Week 8-9
Separation of the oral and nasal cavities

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11
Q

processes of the developing face, arch?

A

The developing face is represented by the frontonasal region, and the
maxillary/mandibular prominences all derived from the first pharyngeal (branchial) first pharyngeal (branchial) arch.

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12
Q

Frontonasal prominence

A

Tissue surrounding the forebrain.

Neural-crest derived mesenchyme from arch 1.

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13
Q

max and man prominence from what arch

A

arch 1

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14
Q

dorsal to the first arch elevation?

A
elevation formed by 
the underlying trigeminal 
ganglion, the sensory 
ganglion for the nerve 
that supplies tissues 
derived from the first 
arch.
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15
Q

nasal placodes

A

formed week 5 from the medial and lateral nasal prominences

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16
Q

req for normal upper lip dev?

A

Union of the nasomedial prominence with the nasolateral prominence and maxillary prominence is required for normal development of the upper lip.

17
Q

intermaxillary segment

A

btwn max prominences, gives rise to the philtrum

18
Q

nasolacrimal and parotid duct development

A

NL: develops where the max and NL prom meet
Parotid: develops btwn the max and man prom

19
Q

palatogenesis

A

weeks 5-12
union of NM prom to form the primary palate
union of maxillary palatal shelves to the form the secondary palate
both primary and secondary join to for the palate

20
Q

what structure is found where all three palatal processes join, content?

A

incisive foramen

nasopalatine nn

21
Q

what must move for palatal fusion

A

nasal septum-up

tongue- down

22
Q

bifid uvula

A

also possible from a lack of fusion at the palatal shelves, often not an issue but can indicate submucosal cleft in some cases

23
Q

fusion of the palate seperates?

A

oral and nasal cavities

24
Q

oro-facial clefts, types

A

 Separation or opening in a structure of the face
 Cleft lip (gingiva, alveolus of the maxilla)
 Cleft palate (hard, soft)
 Isolated (CL or CP) or combined (CL/P)
 Unilateral or bilateral
 Atypical clefts (median, transverse, oblique)

25
Q

cleft lip types

A
26
Q

cleft palate, issues with/treatment?

A
Palate only affected – primary or secondary/incomplete or 
primary+secondary=complete cleft
 Feeding problems
 Surgical intervention at 9-
18 months
 Speech pathologist
27
Q

Submucous Cleft Palate

A

 Only the uvula (soft palate) is affected

 Can result in muscular abnormalities

 Repair if speech is affected

28
Q

Complete Cleft Palate

A

 A complete cleft palate involves a cleft of the palate
and the alveolus.
 Open communication between oral & nasal cavities.
 Bone grafts are required
 Orthodontic treatment is required

29
Q

Complete Cleft Palate, Bilateral

A

 A complete bilateral cleft palate leaves the premaxilla unattached, allowing it to grow forwards.
 Premaxilla and carries the upper four central teeth.
 A double bone graft at the time the permanent teeth are erupting is required for this type of cleft.

30
Q

what additional structure that we know can be affected by clefts?

A

ET

31
Q

facial cleft are often associated with what syndromes

A
Cleft lip and palate are frequent components of 
syndromic disorders (chromosomal abnormalities)
32
Q

Pierre Robin Sequence with cleft

A

pushed back tongue may obstruct the palatal shelves from fusing leading to a cleft palate