Craniofacial Disorder Slide Deck Flashcards

1
Q

McGurk Effect

A

Cocktail party effect

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2
Q

Its not just the syndrome or disorder..

A

its the individual with a syndrome or deformity

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3
Q

Beckwith-Wiedmann Syndrom

A

-overgrowth syndrome: macroglossia
-hemihyperplasia
-cancer risk
-abdominal wall defect
-often born premature (54%)

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4
Q

risk factors for communication disorders

A
  • hearing impairment
  • ear infections
  • cleft palate
  • global developmental delay
  • long term tracheostomy
  • prematurity
  • problematic hyperglycemia
  • fetal toxin exposure
  • family history of communication disorder
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5
Q

BWS study found

A

Those with more risks needed the speech therapy

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6
Q

possible manifestations of untreated macroglossia

A

labial flaring of anterior teeth
increased interdental spacing
anterior open bite
mandibular prognathism

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7
Q

post operative speech for macroglossia

A

-back to baseline speech in 1-6 weeks
-children who required speech therapy before also need it after

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8
Q

conclusions

A

-macroglossia may not be the cause of a speech disorder
-tongue reduction surgery may not prevent a speech disorder
- presence and severity of speech language and feeding disorder is more strongly related to other risks

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9
Q

sagittal synostosis

A

-premature closure/congenital absence of sagittal suture
-elongated skull
-narrow face

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10
Q

corollaries

A

what seems benign may not be as benign as we think, what seems catastrophic may not be at all

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11
Q

what does the patient bring to the evaluation

A

learn about the syndrome, learn about the patient!

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12
Q

craniosynostosis

A

premature fusion or congenital absence of one or more of the cranial sutures

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13
Q

unicoronal synostosis

A

plagiocephaly or twisted skull
progressive facial asymmetry if untreated

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14
Q

bicoronal synostosis

A

rare disorder
facial symmetry maintained
brachiocephaly
subtle language differences
language evaluation at age 4

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15
Q

metopic synostosis

A

trigonocephaly
50% language disorder learning or behavior disorder

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16
Q

other craniosynostosis

A

lambdoid, squamosal, combination of sutures

17
Q

crouzan syndrome

A

+- craniosynostosis
autosomal dominant
fibroblast growth factor receptor 2 gene
hyperplastic midface
normal cognition
some have articulation or language disorder

18
Q

Pfieffer syndrome

A

midface hyperplasia, craniosynostosis, broad thumbs, normal cognitive function

19
Q

Apert syndrome

A

midface hypoplasia, multiple craniosynostosis, syndactyly of digits, some have cleft palate, cognitive range of MR mild to normal,

20
Q

isolated cleft lip (primary palate only)

A

high prevalence middle ear disease, 25% in speech therapy, language and phonological disorders