Torticollis/Genetics/Spine Flashcards

1
Q

Risk factors for torticollis. What are the most common?

A
  • large birth weight
  • male
  • multiple births
  • primiparous mother (1st pregnancy and 1st birth)
  • use of vacuum or forceps assist
  • nuchal cord
  • maternal uterine abnormalities

Most common

  • difficult labor and delivery
  • breech position
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2
Q

torticollis is associate with what

A
  • hip dysplasia
  • clubfoot
  • CBPI
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3
Q

Torticollis is an initial sign in __________ tumors.

- What are symptoms?

A

posterior fossa

- symptoms of headache, nausea, and vomiting

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4
Q

What are the 4 subtypes of torticollis?

A
  • SCM tumor
  • Muscular torticollis
  • Postural torticollis
  • Postnatal torticollis
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5
Q

SCM Tumor torticollis characteristics

A
  • discrete mass palpable on SCM
  • normal x-ray
  • tissue changes - fibrosis, hyperplasia, and atropthy
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6
Q

Muscular torticollis characteristics

A
  • tightness but no palpable mass
  • normal x ray
  • head tilt, ROM limitations, cervical muscle imbalance
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7
Q

Postural torticollis characteristics

A
  • no mass, no tightness of SCM
  • normal x ray
  • head tilt, no PROM limitations, AROM limitations, cervical muscle imbalance
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8
Q

What are possible causes of congenital muscular torticollis?

A
  • benign paroxysmal torticollis
  • congenital absence of cervical muscle(s) or transverse ligament
  • contracture of other neck muscles
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9
Q

Postnatal Muscular torticollis characteristics

A
  • environmental induced (laying on same side)
  • plagiocephaly induced (asymmetrical head)
  • positional preference induced
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10
Q

Which subtype of torticollis will have A/PROM limitations and which subtype will only have AROM limitations?

A

A/PROM limitations - muscular torticollis

AROM limitations only - Postural torticollis

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11
Q

What is the sign for plagiocephaly?

A

Anterior progression of the ear on the same side as the flattened occiput

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12
Q

Brachycephaly

A

a condition where the head is disproportionately wide

- Baby who spends a lot of time on their back

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13
Q

Scaphocephaly or dolichophaly. What population is this common in?

A

a condition where the head is disproportionately long and narrow

Common in babies born prematurely

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14
Q

craniosynostosis. What can this result in?

A

early fusion of the suture of the bones of the skull

- may result in increased cranial pressure

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15
Q

shape of lamboid craniosynostosis head

A

skull takes on trapezoid shape (wider in front, narrower in back)

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16
Q

What are the associated changes in body structure with torticollis?

A
  • decreased ipsilateral cervical rotation
  • decreased cervical lateral flexion

favor extension

  • Will lack flexion and midline control
  • May favor ATNR to side they are facing and may neglect other side
  • Will not like tummy time
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17
Q

Red Flags in Initial Presentation of Torticollis in Children (9)

A
  • age of presentation greater than 6 months
  • pain
  • neurologic findings
  • associated syndromes (down, skeletal dysplasia)
  • trauma
  • inflammatory or infectious history
  • alternating sides
  • atypical position
  • late onset
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18
Q

Motor Characteristics of Children with Torticollis

A
  • supine - trouble centering head to midline
  • bias towards extension and asymmetry
  • visual gaze toward side of head turning
  • prone - altered forearm weight bearing
  • cascade - abdominals, trunk and extremity righting
19
Q

normal PROM neck rotation and lateral flexion for babies

A

neck rotation - 110

lateral flexion - 70

20
Q

What is the muscle function scale?

A
  • used to assess torticollis - football hold baby
    1-6 scale with 1 (head held significantly below horizontal line/most severe) to 6 (head held significantly higher above horizontal line/least severe)
21
Q

indications for a TOT collar

A
  • 4 months or older
  • constant tilt of 5 deg or greater for more than 80% of awake time
  • perform all movement and motor skills w/ tilt
  • adequate ROM and head tilting reactions
22
Q

discharge guidelines for torticollis

A
  • full PROM and AROM
  • maintain midline 95% of time
  • no compensatory pattern
  • = and age appropriate head righting
23
Q

contraindications for cranial orthoses

A
  • craniosynostosis
  • unshunted hydrocephalus
  • children beyond 18 months of corrected age
  • babies under 3 months of age
24
Q

Monogenic, polygenic, cytogenetic

A

mono - single gene involved

poly - many genes involved

cyto - large-scale changes in chromosomes

25
What are the 4 categories of genetic disorders?
- chromosomal - not hereditary - single gene - multifactorial - mitochondrial
26
chromosomal disorder
deletions, inversions, duplications, translocations | - not hereditary
27
signs of down syndrome
cloudy eyes | horizontal line across palm
28
_________ is most common health problem with 40% having malformations in down syndrome
coronary heart disease | - cardiovascular issues
29
What is Turner and Klinefelter?
sex chromosome disorders - Turner (1 X chromosome - female) - Klinefelter (2 X and 1 Y chromosome - male)
30
Marfan's syndrome has what type of issues?
CV issues
31
Cri-du-Chat
cat like cry as infants | - low birth weight, hypotonia, cognitive impairments, clumsiness
32
Prader Willi
- excessive eating by 2 years of age | - behavior issues
33
occulta spina bifida
- failure of vertebral arches to meet & fuse in 3rd month - Overlying skin may be marked by dimple, pigmentation, or patch of hair - no neurological or MSK dysfunction
34
meningocele or myelocele
- spinal cord vertebral canal but may be abnormal
35
myelomeningocele
extensive spinal cord abnormalities | - spinal cord and meninges out of vertebral canal
36
anencephaly
cranial end of neural tube does not fuse
37
bulging fontanelle and sunset sign are signs of what
shunt malfunctioning in infants
38
What is arnold chiari malformation? What are symptoms?
brainstem and cerebellum herniate through foramen magnum | - respiration, paralysis of vocal cords, apnea, swallowing, abnormal gag, UE weakness
39
What is hydromyelia? What are symptoms?
dilation of the center canal of spinal cord | - rapidly progressive scoliosis, UE weakness, spasticity, ascending motor loss in LE
40
What is tethered cord? What are symptoms?
pathological fixation of the spinal cord in an abnormal caudal location - decreased strength, LE spasticity, back pain at sit of sac closure, change in urological function
41
What can flaccid LE or frog leg position cause?
hip abduction tightness which can limit movement from sitting to quaddrapped
42
what muscles are strong in high lumbar kids? What does this put them at risk for?
strong hip flexors and adductors | - increased risk for dislocations
43
What muscles are strong in low lumbar spinal injury kids?
- strong hip flexors and adductors - some hip abduction - strong quads and medial hamstrings - anterior tib and some foot intrinsics
44
What muscles may be weak with sacral level spinal injuries? What may this cause?
gastroc weakness - need AFO for gait | - can lead to crouched gait and increased weight gain