Developmental Neuro Flashcards

1
Q

What is the diagnostic criteria for DCD

A

learning and coordinated movement is difficult
early onset of development
all other neuro issue been ruled out
difficulty with motor that intefere with ADLs

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2
Q

What is a specific test and measure for DCD partication?

A

CAPE (childrens assessment of participation and enjoyment)
goal attainment scale
canadian occupational performance measure

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3
Q

What are DCD diagnosis specific tests?

A

DCD’Q’07 age 5-15
movement assessment battery for children-2 = gold standard
<5th % on MABC2– probable DCD

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4
Q

What activity limitation test and measure for DCD?

A

motor development – BOT 2

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5
Q

What age should you do individual PT for children with DCD?

A

<5-6

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6
Q

WHat is the CO-OP

A

cognitive orientation to daily performance (CO_OP)
7 key features =
guided discovery,
client chosen goals,
dynamic performance analysis (DPA)
parent involvement
structured interventional formal 10-12 sessions.

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7
Q

What age do you focus on group therapy sessions

A

> 6 years old

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8
Q

What intervention specific to DCD?

A

CO-OP
neuromotor task training
motor imagery

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9
Q

Is there a medical management for DCD

A

no medications, but can treat co-morbidities

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10
Q

What is the diagnostic criteria for autism?

A

DSM-V
impairment in social communication/interaction
restricted/repetitive behavior

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10
Q

What is the classification of level of support

A

level 1= support
level 2= mod support
level 3= substantial support

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11
Q

What is the pathophysiology of autism?

A

synapses do not undergo normal pruning during childhood and adolescense
cerebral morphology differences in volume and geometry
brains of indiviudals with autism are large
overgrowth in temporal lobe

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12
Q

What are common co morbid conditions of autism

A

ADHD, OCD, DCD, anxiety/ mood, psychosis

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13
Q

What are predictive factors for autism?

A

geriatric pregnancy, medications during pregnancy, air pollution, genetics

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14
Q

What is the medical management for autism?

A

no specific, but can managed other medical conditions

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15
Q

What is autism diagnostic observation schedule (ADOS)?

A

gold standard– completed by psychologists, along with clinial observation
semi structured assessment of communication, social interaction and play for individuals
4 modules– child to adult

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16
Q

What is the screening for autism

A

M-CHAT-R used for 6- 30 months

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17
Q

What are interventions for autsim?

A

focus on meaningful interventions
short duration
ICF components
accomodate environment
integrate interventions with daily routines

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18
Q

What is a common impaitment or deviation for children with autsim?

A

idiopathic toe walking

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19
Q

What is idiopathic toe walking?

A

condition in which children ambulate with bilateral toe-toe pattern without known etiology

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20
Q

What are interventions for idiopathic toe walking?

A

behavioral strategies (flippers, heels, squeakers)
followed by serial casting followed by orthotic

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21
Q

What is spina bifida

A

type of neural tube defect

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22
Q

When does the caudal neural tube close?

A

day 28

23
Q

When does the rostral neural tube close?

A

day 24

24
Q

What is the double hit theory

A

maldevelopment of the neural tube + exposure to amniotic fluid= damage to normal spinal cord tissue

25
Q

What are risk factors for spina bifida?

A

polycentric inheritance
envirnmental
follic acid deficeincy

26
Q

How do you diagnose spina bifida?

A

lab alpha- fetoproteint at 13-15
fetal ultrasound 16-24 wks
amniocentesis at 16-18

27
Q

Which diagnostic test is 100% accurate?

A

amniocentesis

28
Q

What is a banana sign?

A

cerebellum appears banana like because it is wrapped around the posterior brainstem due to downward traction of the spinal cord
indicative of Chiari II

29
Q

What is a lemon sign?

A

is the shape of the skull

30
Q

What are the different types of spina bidfia

A

myelomeniongecele
meninogecele
myocele
spina occulta

31
Q

Describe myelomeningocele

A

most common
nerves outside spinal tract– open defect
motor, sensory, bowel and bladder impairments
majority 75% lumbar-lumbosacral

32
Q

Decribe meningocele

A

incomplete skin coverage= CSF leak
neuro signs may normal
pocket but no nerve elements

33
Q

Describe myelocele spina bifida

A

cystic cavity anterior to the spinal cord
majority 75% lumbar-lumbosacral

34
Q

Describe occulta spina bifida

A

L5-S1 is most common
no neurological deficits
rarely associated with tehtered cord or lipoma

35
Q

what is hydrocephalus?

A

CSF build up in the ventricles

36
Q

what is tethered cord?

A

spinal cord gets stuck to the base of spine
w/ growth SC can’t move

37
Q

What is syringomyelia

A

pockets of fluid throughout the spinal cord

38
Q

What is Arnold Chiarir Type II Malformation ?

A

downward displacement of medulla, brainstem and cerebellar tonsil through fooramen mangnum

39
Q

What are the symtpoms of arnold chiari type II?

A

sleep apnea
palpitations/arrhythmis
diploplia
dysphagia
impaired fine motor coodination and ataxia

40
Q

What are the symptoms of hydrocephalus?

A

HA
nausea
altered mental status
lethargy
personality change
swallow issues
hoarse cry
vision changes

41
Q

What are the symptoms syringomyelia?

A

motor changes (fine motor)
sensory changes (temperature)
reflex changes
neck pain

42
Q

What are symptoms of a tethered cord?

A

motor, sensory, reflex change
back pain
progressive scoliois
bowel or bladder/ sexual changes
change in function

43
Q

What is the sign or gaze palsy associated with severe hydrocephalus?

A

sunset gaze
upward gaze palsy

44
Q

what is the most frequent shunt complication

A

infection

45
Q

When do children with thoracic level SB roll?

A

18 months

46
Q

What are the predictors of ambulation?

A

lower motor level
no histroy of shunt
no hx of hiip or knee contracture surgery

47
Q

what are the cuntional abilities for thoracic level?

A

standing at 12-18 months
gait with HKAFO
wheelchair training as early 12 months

48
Q

Functional abilities of lower thoracic and lumbar

A

RGO after age 3
if L3 spared – child may use AFO

49
Q

Functional abilities of low lumbar aand sacral

A

bracing may not be required but might benefit from AFO or GRAFO if PF are non-functional

50
Q

What is common impairment in the feet for T6-T12

A

club foot

51
Q

What is a common gait pattern you might see with a patient with an L4 myelomeningocele?

A

trendelenburg

52
Q

What are common orthopedic conditions for spina bifida

A

scoliosis
clubfoot
hip subluxation and dislocation

53
Q

What is neurogenic bowel?

A

surgery required for patient with difficulty with independence and maintaining continenence
80% of kids have it

54
Q

what is a neurogenic bladder?

A

present in >90% patients with MMC
hypertonic bladder= thoracic lesions
hypotonic= sacral lesions
need annual renal ultrasouns and renal function testings

55
Q

What is the management for neurogenic bladder?

A

management= normal renal function and maximize continende
independent catheteization as early as 5/6 years old
UTI ver common
urologic cause 40% deaths between 5-30 years old

56
Q

What are common considerations for skin care for spina bifida?

A

allergy to latex
high risk for pressure injuries