lecture Qs final Flashcards

(38 cards)

1
Q

torticollis

A

abnormal twisting of the neck which causes the head to be held in a rotated or tiltled position
75% right side

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2
Q

muscular causes of torticollis

A

fibromatosis colli
muscle spasm following trauma
just trauma

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3
Q

cause of torticollis(broad)

A

Muscular or Skeletal

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4
Q

cause of torticollis skeletal

A
unilateral interfacetal dislocation UID
occipital condyle fracture
Atlanto -axial rotatory fixation 
cns related
subarachnoid hemorage
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5
Q

Fibromatosis colli

A

rare but accounts for 80% of childhood torticollis
due to traumatic delivery &
positioning in utero- develops 2-3wks after birth

benign proliferation of fibous tissue into SCM lower 1/3

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6
Q

Bezold’s abscees

A

complication of suppurative mastoiditis

Occurs when infection errodes the mastoid tip into the neck, forming an abscess — can result in torticollis*

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7
Q

true or false

torticollis can be caused by Rheumatoid Arthritis

A

true

due to Pannus

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8
Q

most common sagittal synostosis

A

doliochocephaly (sagittal synosis

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9
Q

sagittal synostosis

A

Boat head/ scaphoscephaly(broad term 4 sagital)

used to describe a narrow head shape

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10
Q

Coronal synostosis unilateral

A

Bent-Head( Plagiocephaly)

More on left

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11
Q

if coronal synostosis bilateral

A

brachycephaly

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12
Q

metopic synostosis

A

triangle -head ( trigonocephaly)

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13
Q

lamboid synostosis

A

slant head- Occipital plagiocephaly

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14
Q

scaphocephaly

A

most common form of craniosynostosis; more common in males

premature closure of sagittal suture

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15
Q

Trigonocephaly

A

premature closure of metopic suture

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16
Q

turricephaly

A

premature closure of coronal suture

17
Q

Frontal plagiocephaly

A

2nd most common craniosynostosis

18
Q

Occipital Plagiocephaly

A

More common in immobile children

premature closure of lamboid suture on one side

19
Q

syndromic craniosynostosis

A

autosomal dominant linked to chromosome 10q

20
Q

FGFR

A

(fibroblast growth factors)important in angiogenis
related to craniosynostosis syndromes
binds to many receptors
will see too much bone formation

21
Q

FGFR1

A

pfieffer syndrome

22
Q

FGFR2

A
HOTTEST fibroblast gene for mutations:(learn 1 &3 easier)
crouzon syndrome
Apert Syndrome
Prieffer syndrome  
Jackson wies syndrom
23
Q

FGFR3

A

Achondroplasia

thanstophoric dysplasia

24
Q

primary craniosynotosis

A

abnormal biology of the suture causes premature suture closure- FGfR related craniosynotosis

25
secondary craniosynotosis
suture biology is normal | but abnormal external forces result in premature suture closure
26
crouzon sydrome
``` craniofacial dysostosis complete penetrance autosomal dominant 50%due to spontaneous mutations Due to mutation of FGFR-2gene =10q26* NO SYNDACTYLY or cervical fusion ``` class 3 , midface hypoplasia
27
apert
autosomal dominant | FGFR2- gene 10q26
28
Pfeiffer's syndrome
skull is prematurely fused and unable to grow normally -craniosynostosis Bulging wide set eyes due to shallow eyesockets FGFR-2 under developed mid face
29
Muenke syndrom
phenmotypic overlap occurs with other disease intellect normal Characterized by coronal synostosis or macrocephaly
30
jackson wiess syndrom
foot abnormalities and premature fusion of certain parts of the skull
31
ventrolateral
early migration trunk neural crest cell.. they migrate into and through the anterior of half of each somite
32
vagal and sacral neural crest generate what
parasympathetic(enteric) ganglion
33
Cardiac neural crest cells form
Endothelial lining
34
where does heart form
ink neck under pharyngeal arches
35
cranial(cephalic) neural crest cells
cells from craniotomy facial mesenchyme ; | creates facial cartilage and bone
36
neuro plate folds and forms
neural tube
37
poor saliva affects which arch more
Mandibular
38
poor saliva causes
more friction at the denture mucosa interface