Download - Dyskinesias in Children/Adolescents CPT Timothy L. Switaj, MC, FS, USA Neurology (Child) Intern
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Dyskinesias in Dyskinesias in Children/AdolescentsChildren/Adolescents
Dyskinesias in Dyskinesias in Children/AdolescentsChildren/Adolescents
CPT Timothy L. Switaj, MC, FS, USACPT Timothy L. Switaj, MC, FS, USANeurology (Child) InternNeurology (Child) Intern
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Objectives• To demonstrate the basic abnormal
movements in children/adolescents• To begin to think about a differential
for each type of movement• Brief discussion of the most likely
etiologies of the abnormal movements
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Basic Movement Types• * Chorea/Athetosis
– Ballismus• Dystonia• Hemifacial Spasm• Mirror Movements• * Myoclonus• Stereotypies• * Tics• * Tremor• Fasciculations• Myokymia• Seizures
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Things to ask yourself when seeing patient
• What does the movement look like?– Is it rhythmical, jerky or “dancelike”?
• Can it be suppressed?• What medications is the patient
taking?• Any Family History of similar
movements?
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General Characteristics (1)
• Chorea/Athetosis – usually seen together– Chorea – rapid movement affecting body part that is
incorporated into voluntary movement to hide it, NO FIXED FORM
• Constant movement (restlessness)• Movements flow from side to side and limb to limb
– Athetosis – slow, writhing movement of the limbs• Can occur alone but usually associated with chorea –
athetosis without chorea is due to perinatal brain injury (most likely perinatal asphyxia)
– Ballismus – high-amplitude, violent flinging of a limb (an extreme form of chorea)
– Tardive Dyskinesia – uncommon in children
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General Characteristics (2)
• Dystonia – sustained muscle contractions– Can be focal, segmental, hemi or generalized
• Hemifacial spasm – involuntary, irregular contraction of muscles innervated by one facial nerve– Very rare in children
• Mirror movements – involuntary movements of one side of body that are mirror reversals of intended movements on the other side– Normal during infancy and disappear before
age 10 – persistence can be familial trait– Obligatory movements are abnormal at any age
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General Characteristics (3)
• Myoclonus – involuntary movements characterized by rapid muscle jerks– Can be rhythmic, nonrhythmic; focal,
multifocal or generalized; spontaneous, action or reflex
• Stereotypies – repeated, purposeless movements– Can be simple or complex
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General Characteristics (4)
• Tics – “habit spasms”; complex, stereotyped movements or utterances that are sudden, brief and purposeless– As opposed to chorea, are stereotyped– Can be suppressed for short periods,
with some discomfort and are never part of a voluntary movement
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General Characteristics (5)
• Tremor – involuntary oscillating movement with a fixed frequency– Product of frequency and amplitude
are constant• Frequency decreases with age,
amplitude increases
– Shuddering, ataxia and dysmetria are not tremor because they lack rhythm
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General Characteristics (6)
• Fasciculations– Rippling movements of a small group of
muscles, benign with low amplitude common in young
• Myokymia– Slow, worm-like, undulating movements
usually in the face but also in the large limb muscles
• Seizures
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Chorea - Differential• Neurodegenerative diseases (Huntington’s)• Lesions of the basal ganglia• Drugs (Dopamine agonists, stimulants, opiates,
antiepileptics, estrogens)• Metabolic conditions (Wilson’s, hyperthyroid,
hyperglycemia, hypoglycemia, electrolyte disorders)
• Systemic disorders (Syndenham’s, lupus, chorea gravidarum)
• Essential chorea syndromes• Paroxysmal chorea• Cardiopulmonary bypass (1 to 10%)
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Huntington’s - Genetics
Autosomal dominant, full penetrance, 50% chance to pass toOffspring, CAG repeat of greater than 39 is diagnostic
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Huntington’s - Features• Age of onset typically 35-45, but
childhood to >80 has occurred• Chronic, progressive, generalized chorea• Failure of indirect pathway• Can have other movement disorders
present (parkinsonism, dystonia and tic)• Dementia late in disease
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Syndenham’s - Features
• A.K.A. Rheumatic Chorea• 10 to 30% of cases of rheumatic fever• Symptoms appear 1 to 6 months after infection
and last 5 to 15 weeks• Recurs in 20% of patients• Can cause mental status changes• Most cases in ages 5 to 15• Migratory chorea of limbs and face• Cardinal features of chorea, hypotonia, dysarthria
and emotional lability• Treatment with steroids and treatment for infection
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Chorea Gravidarum• Due to antiphospholipid antibody
syndrome, with or without SLE• Usually during 2nd to 5th month,
sometimes postpartum• Cognitive changes may be present• Symptoms resolve spontaneously
in weeks to months
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Chorea – workup/treatment
• Neuroimaging, glucose, electrolytes, thyroid studies, CBC with smear, copper studies, genetic studies
• Treat underlying cause• Can use clonazepam as first line• Neuroleptics are second line• Follow-up important because chorea
tends to evolve
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Myoclonus - Evaluation• Distribution
– Generalized, focal, multifocal, segmental
• Temporal profile– Continuous, intermittent
• Activation– Rest, voluntary, stimulus
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Myoclonus - classification
• First – determine major category• Second – match clinical and
lab/radiology findings with diagnosis within major category
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Myoclonus - Categories• Physiological• Essential• Epileptic• Symptomatic
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Myoclonus - Physiologic• Neurologically normal persons• Sleep jerking – most common• Also be anxiety or exercise related• Diagnosis based on history alone• NO TREATMENT NEEDED
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Myoclonus - Essential• Clinically significant jerking occuring at any time• Usually most prominent or only finding• Differs from physiologic because of social or
physical disability• Condition progresses slowly or not at all• Hereditary (Autosomal dominant) or sporadic• Face, trunk and proximal muscles• Clinical features and family history make
diagnosis• Clonazepam drug of choice is treatment needed
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Myoclonus - Epileptic• In persons with chronic seizure disorder
and epileptiform activity on EEG• Juvenile Myoclonic Epilepsy
– Myoclonic seizures with generalized tonic-clonic or absence
– Onset in adolescence with peak between 12 and 18
– Abnormality on chromosome 6
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Myoclonus - symptomatic
• Neurodegenerative syndromes• Infection/Postinfection• Drugs, toxins, metabolic disorders• Hypoxia• Focal or segmental• Paraneoplastic• Post-CNS injury
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Myoclonus – workup/treatment
• Electrolytes, glucose, renal and hepatic function testing, drug and toxin screening, brain imaging, EEG
• Genetic studies, tissue biopsy and CSF studies as clinically indicated
• Treatment is clonazepam• Valproic acid for JME
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Tics• Can be suppressed for short
periods of time• Simple or complex• Transient tics occur in 20% of
children under 10 years of age• Gilles de la Tourette syndrome
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Tourette’s• 10 cases per 10,000 population• Onset between 2 and 15 (mean 6.5)• Vocal tics begin 1 to 2 years after motor tics• 75% are tic free by 18 years old• Increase in severity with stress, caffeine, stimulants,
fatigue, heat, steroids• Decrease with THC, alcohol, nicotine and decrease in
mental activity• Disability usually social but may be physical injury• 50% also with ADHD, 30 to 50% with OCD• Multiple other behavioral problems
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Tourette’s• Diagnosis:
– Multiple motor and one or more vocal tics– Onset before age 18– Tics occur many times a day, nearly every
day– Variation in location, frequency and
complexity over time– Not related to toxins or CNS disease– Symptoms cause impairment
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Tourette’s• Genetic factors in 75% with bilineal
transmission in 25%• Radiologic/Laboratory workup not
needed• Treatment
– Clonidine, benzodiazepines, haldol, risperdal, clozapine, reserpine
• Surgery for drug-resistant tics, but not shown effective in Tourette’s
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Tremor• All people have a physiologic
tremor inherent in movement that cannot be normally noticed unless measured
• Fine or coarse• Resting, postural, action
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Connor GS et al. Esential Tremor: A Practical Guide to Evaluation,Diagnosis, and Treatment. Clinician, 19(2): 2001.
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Tremor - differential• Drug induced (Anticonvulsants,
antidepressants, caffeine, steroids)• Hyperthyroidism• Juvenile Parkison’s disease (Not
common)• Paroxysmal Dystonic Head Tremor• Essential tremor
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Essential tremor• 1 in 20 arise in childhood• 70% of pediatric cases in males• Not associated with other neurologic
disturbances• Genetics – ETM1 on 3q13, ETM2 on 2p25,
complete penetrance, autosomal dominant• Most common movement disorder• Prevalence of 0.1 to 22% worldwide• 20 times more common than Parkinson’s
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ETM1 – Chromosome 3q13
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ETM2 – Chromosome 2p25
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Essential tremor - Features
• 4 to 8 hertz• Usually in limbs, occassionally head and face• Appears first in hands because it is enhanced by
greater precision movements• Can be postural (early) and action (later)• Generally life-long• Can impact writing and other functions• Worsening due to enhanced physiologic tremor• Enhanced by anxiety, attempts to suppress, fatigue• Tremor can become severe with significant
disability
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Connor GS et al. Esential Tremor: A Practical Guide to Evaluation,Diagnosis, and Treatment. Clinician, 19(2): 2001.
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Essential Tremor – workup/treatment
• Neuroimaging normal, pathology not indicated, genetic research possible if familial
• Treatment usually not needed• If needed use beta-blockers first
– Then anticonvulsants, benzos, calcium channel blockers, botox
• If severe tremor, drug-resistant, deep brain stimulation
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DBS - Thalamus
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DBS - Localizing
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DBS - Leads
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References• Postgraduate Medicine, 108(5), Oct
2000.• Pranzatelli MR. Movement Disorders
in Childhood. Ped Rev, 17(11): 1996.• Gerald M. Fenichel. Clinical Pediatric
Neurology, 4th Edition. 2001.• All videos courtesy of Dr. DifazioAll videos courtesy of Dr. Difazio