Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
44 Cards in this Set
- Front
- Back
pediatric neuro exam- history
|
1. birth hx: prolonged delivery, preg issues, illnesses
2. developmental hx: nml milestones, special ed classes? 3. FH 4. immunizations 5. PMH 6. allergies 7. Recent travel, illnesses |
|
general exam
|
-look at them, play with them
-facies? -syndromic appearance? -dysmorphic features? -skin- neurocutaneous lesions |
|
Brushfield spots
|
- in downs syndrome
-whitish or light grey or brown spots in the eyes |
|
Angelman Syndrome
"happy puppet" |
-maxillary hypoplasia
-large mouth -prognathism -mental retardation -autistic features: poor eye contact, speech delay -inappropriate outbursts of laughter -flickering tongue -ataxia gait -15q11-q13 deletion on maternal chromosome |
|
Fragil X
|
-long, wide protruding ears
-elongated face -flattened nasal bridge -large testes -CGG triplicate repeat -developmental delay -predominately male |
|
General congenital malformations
|
-possible neural tube defects
-inspection of the spine and lumbo-sacral region of back...look for... 1. sinus tracts/dimples 2. hair tufts 3. raised skin covered bumps 4. Meningocele/ Myelomeningocele/ Encephalocele |
|
neural tube defects
|
most severe: no brain formation (anencephaly)- do not survive
less severe: partial failure of anterior closure - encephalocele less severe- partial failure of post closure- meningocele, spina bifida -prevention most impt tx! -folate taken before preg! |
|
Skin- Sturge-Weber Syndrome
|
-neurocutaneous syndrome
-skin can be a reflection of the brain -Facial hemangioma-most freq in V1 and V2 distribution (may be little) -seizures -contralateral hemiplegia -mental retardation (50%) -need MRI |
|
Cafe Au lait spots neurofibromatosis type 1
|
-large freckles
- in place where "sun doesnt shine"-axillay -deeper color than skin -6+ spots, grow with age |
|
neurofibromatosis type 1
|
2+ signs:
-cafe-au-lait spots -2 neurofibromas -intertrigonal freckling -sphenoid wing dysplasia or congenital long bone bowing -B/L optic gliomas! (tumors on optic nerve, will lose vision) -2 lisch nodules-pigments in iris, benign -1st degree relative w/NF -epilepsy, learning d/o, hydrocephalus -need MRI or CT |
|
Developmental exam
|
-Denver developmental screen
-more like playing -remember to correct age of premature babies for testing -There are age defined expected milestones in areas of social, gross motor, fine motor and language |
|
M-CHAT (Modified Checklist for Autism in Toddlers)
|
-to screen kids for further testing for autism
1. Social interactions: doesn't look at you, has no peer relationships, lack of emotion 2. Communication: lack of expression, lack of imaginative play, cannot make needs known 3. Stereotypies: inflexibility, repetitive movements, restricted interests, preoccupation w/parts of objects |
|
Pervasive Developmental DisordersAutism Spectrum Disorders
|
-cannot be attributed ot another disorder
-delays or abnml social skills before age 3 -6+ more features for 3 major areas: social impairment, communications impairment, restricted repetitive and stereotyped behaviors |
|
Head circumference
|
-avg at birth: 35 cm
-inc by 2cm/mo for 0-3 months -inc by 1cm/mo for 3-6 months -premees grow faster |
|
Mental status
|
1. altertness
2. attentiveness 3. language 4. behavior- interaction with you, parents, siblings 5. enviornment 6. age appropriateness 7. follows commands? |
|
Cranial nerves
|
1. Eyes-gaze, nystagmus, acuity, visual fields, tracking, fundoscopic
2. olfactory- s/p head trauma 3. CN VII- facial nerve- bells palsy 4. CN III, IV, VI- EOM 5. stick out tongue 6. open-say "aahh" 7. infant- put a gloved finger in the mouth, how well do they suck? |
|
Pseudopapilledema
|
-pt with farsightedness
-difficulty seeing up close -blurred distance vision -eye fatigue when reading -eye strain -crossed eyes in kids |
|
Facial motor pathway
|
-upper face muscle have bilateral control
-lower face muscles have only ipsilateral control -worse looking if peripheral lesions (True Bells Palsy) |
|
Facial weakness
|
-cannot close L eye
-L peripheral CN VII lesion -on LI r/o lyme disease -LP recommended -CT scan first |
|
plantar reflex
|
-babies will fan out until about 1 yr old
|
|
Guillain-Barre syndrome
|
-ascending weakness, no reflexes
-almost always preceding viral illness (EBV, CMV, Herpes, Mumps) or post vaccine (varicella) -monitor for respiratory compromise -miller-fischer variant: descending weakness w/triad of areflexia, ataxia and opthalmoplegia) -tx: TVIG |
|
newborn reflexes
|
-slides!
|
|
Charcot-Marie-tooth
|
-hereditary motor sensory neuropathy
-decreased proprioception and pallesthesia -areflexia -foot drop -flat feet -stork legs -problem with myelination, IB more severe than IA |
|
Infant motor and tone
|
-look at baby- frog legs, not moving much
-try to lift - arms should flex if nml - they should provide some resistance -head drops back - cant support or lift it |
|
-Consider Landau Response
|
-(2-3 mo) sustained straightening of head and trunk. Baby can inhibit by 12 months
|
|
Hypertonia
|
1. rigidity: resistance to externally imposed movement throughout the range of motion at any speed
2. Spasticity: resistance to externally imposed movement increases with increasing speed of stretch or beyond threshold joint angle 3. Dystonia: Involuntary sustained or intermittent muscle contractions causing twisting and/or abnormal postures. Painful. |
|
Wilsons disease
|
-liver failure
-hemolytic anemia -low ceruloplasmin -rigidity, dystonia, tremor or tics -kayser-fleischer rings |
|
Tic disorder
|
-boys>girls
-start as a physiologic act that becomes habituated -most outgrow by adolescence -r/o wilsons, iron-def, thyroid, chronic strep -tx: ignore it |
|
Duchenne muscular dystrophy
|
-onset 2-4 yrs
-elevated CPK -calf hypertrophy -X-linked recessive -dystrophin content <3% of nml, death ~20 |
|
Becker muscular dystrophy
|
-onset late childhood
-elevated CPK -calf hypertrophy -x-linked recessive -dystrophin content <20% of nml -less malignant |
|
dysmetria
|
-poor finger to nose
|
|
station and gait
|
Sensory ataxia: stepping gait
Cerebellar ataxia: wide-based Steppage gait: foot drop Spastic hemiparesis: circumduction Spastic paraparesis: scissor gait Dystrophic gat: lordotic w/lateral hip movement (waddle) |
|
Headaches
|
-episodic, chronic
-when to act quickly: new onset, occipital, wakes me out of sleep, neuro signs |
|
Migraines in kids
|
-not usually unilateral,hemiplegic
1. photophobia 2. phnophobia 3. N/V 4. dizzines, fatigue 5. vision changes 6. osmophobia- sensitivty to smells 7. FH, missing school, sleep disturbances |
|
Migraine txs
|
-good sleep, good fluid intake, no caffeine, vitamins, Ca, Mg
-prophylactic tx: antiepileptics, beta blockers, tricyclic antidepressants, Ca channel blockers (>10/mo) -motrin for acute H/A in kids |
|
Attention problems
|
-consider developmental delay and psychiatric disorders
-dx: connor's or vanderbilt screening tests, neuropsyc eval -classroom interventions first -meds if needed (hyperactivity, impulsivity) -omega 3 supplement |
|
Generalized tonic-clonic seizure
|
1. Tonic phase: eyes open & roll up, pupils dilate, elbows flex, arms pronate, incontinence
2. clonic phase: generalized movements, frequency slowly decreases, tongue bitting 3. Post-ictal phase: drowsy, confused, lethargic, HA, muscle sorness |
|
Tonic seizures
|
-flexed/extended, no shaking
-brief |
|
Clonic seizured
|
-Similar to generalized tonic-clonic seizures in nature
|
|
Absence eplilepsy
|
-nml kids
-brief, but can happen many times/day -abrupt recovery -sometimes eyelid flutering |
|
infantile spasms
|
-serious
-look like flexing or extending body repeatedly -occur in clusters when just waking up -nml and abnml kids -usually before 1 yr old -EEG: hypersarrhythmia- chaotic, high voltage discharges -tx: ACTH, Vigabatrin |
|
Simple partial seizure
|
-no loss of consciouness
-can be motor seizures, automatisms -can be sensory -flashbacks -abd discomfort, bradycardia, drooling, hair on end -gelastic- bursts of laughter |
|
Complex partial
|
-loss of consciousness
-temporal > frontal > parietal/occipital -can start as simple partial -automatisms (lip-smacking, gum chewing, nose wiping, buttoning) -can occur with absence -side opposite of focus -may evolve into generalized |
|
Febrile seizures
|
-6mo - 6 yrs old
-generalized tonic-clonic but may be focal -occur with febrile illness -determine cause for fever and tx if needed |