Embryology of the Head, Face and Oral Cavity - Trump 2017 Flashcards

1
Q

when does the central face start to develop?

A

4 weeks starting with the nasal placodes

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2
Q

The upper lip forms from what?

A

the medial nasal processes merging together as well as the maxillary processes merging to those

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3
Q

the primary palate forms from what?

A

the merger of the medial nasal processes

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4
Q

the secondary palate is formed from what?

A

the maxillary process of the first pharyngeal arch

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5
Q

WHat is cleft lip a result of? Is it bilateral or unilateral more often? When conditions need to be met for treatment to begin?

A

defective fusion of the medial nasal process with the maxillary process
80% are unilateral
Tx: lip, rule of 10: 10 weeks 10lbs 10gm %HM

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6
Q

what is cleft palate a result of? when do we treat it?

A

failure of the palatal shelves to fuse

treatment at about 1.5 years

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7
Q

Is it more common to have only Cleft palate or only Cleft Lip? HOw common is it to have both?

A

CP is more common but CL+CP is the most common

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8
Q

For Syndromic clefts what is most common (CL+CP or just CP or just CL)?

A

Cleft palate only is most common for syndromic patients

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9
Q

What is one syndrome we should know where Cleft palate is part of the syndrome? what are the other symptoms of this syndrome?

A

Pierre Robin sequence
CP
Mandibular MIcrognathia
Glossoptosis (downward displacement)

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10
Q

What are the factors involved in non syndromic cleft palate?

A

maternal alcohol or tobacco use
folic acid deficiency
corticosteroid use
anticonvulsant therapy

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11
Q

what causes lateral facial cleft?

A

lack of fusion of the maxillary and mandibular processes

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12
Q

what causes oblique facial cleft?

A

failure of fusion of the lateral nasal processes with maxillary process. commonly associated with Cleft Palate

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13
Q

what causes Median cleft of the upper lip?

A

failure of fusion of the medial nasal processes

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14
Q

what is the most common orofacial cleft?

A

oblique facial cleft

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15
Q

who are the top two races who have the highest prevalence of orofacial clefts?

A

Native Americans and Asians

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16
Q

if you see a bone notch on the posterior hard palate margin and a bluish midline discoloration in the mouth what is likely underneath the epithelium?

A

a submucous palatal cleft

17
Q

T/F commisural lip pits are associated with facial and/or palatal clefts

A

false

18
Q

what type of lip pits are bilateral and are associated with syndromes?

A

paramedian lip pits

19
Q

paramedian lip pits can be associated with what syndrome specifically?

A

van der Woude Syndrome

20
Q

What is the most common form of syndromic clefting?

A

van der woude syndrome

21
Q

What is microglossia? is it usually syndromic? What condition is it usually associated with? What can be missing?

A

abnormally small tongu
usually syndromic
associated with micrognathia
lower incisors may be missing

22
Q

What is Ankyloglossia? Which gender gets it more? What is the treatment? AT what age?

A

having a short thick lingual frenum resulting in limitation of tongue movement
Males more often have it
frenotomy at 4-5

23
Q

What oral structure can house an undescended thyroid gland?

A

the tongue most often

24
Q

Lingual thyroid is more common in which gender? When do symptoms usually arise? Do patients have hypothyroidism?

A

females
puberty
1/3 of patients have hypothydroidism

25
Q

what is the treatment for a thyroglossal duct cyst? what is the presentation of one?

A

removal

presents as a painless, fluctuant, movable swelling at or near midline