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Physiatric findings in individuals with Sturge-Weber syndrome.
|Title||Physiatric findings in individuals with Sturge-Weber syndrome.|
|Publication Type||Journal Article|
|Year of Publication||2010|
|Authors||Suskauer SJ, Trovato MK, Zabel AT, Comi AM|
|Journal||American journal of physical medicine & rehabilitation / Association of Academic Physiatrists|
|Date Published||2010 Apr|
Sturge-Weber syndrome is a rare neurocutaneous disorder that often results in functional impairment caused by motor (typically hemiparesis) and cognitive deficits. A retrospective chart review of physiatric evaluation of 30 individuals, aged 4 mos to 55 yrs (median age, 2.4 yrs), with Sturge-Weber syndrome with brain involvement was conducted for the purpose of summarizing physiatric findings and recommendations in this cohort. Presence or absence of motor, cognitive, and behavioral concerns and need for orthoses, spasticity management, and therapy services were noted. Hemiparesis was common, but the need for intervention for spasticity was rare. Cognitive and behavioral concerns were noted frequently, meriting additional evaluation. Case vignettes are presented to highlight (1) a child with repeated functional setbacks in association with increased seizure frequency who, with seizure control, demonstrated return to functional baseline and subsequent further skill development and (2) a child with Sturge-Weber syndrome who made functional gains with constraint-induced movement therapy.
|Alternate Journal||Am J Phys Med Rehabil|