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Skeletal muscle maximal mitochondrial activity in ambulatory children with cerebral palsy.

Sudarshan DayanidhiElisa H BucknerRobin S RedmondHenry G ChambersSimon SchenkRichard L Lieber
Published in: Developmental medicine and child neurology (2021)
Skeletal muscle mitochondrial electron transport chain enzymatic activity but not mitochondrial content is reduced in independently ambulatory children with CP. Decreased mitochondrial oxidative capacity might explain reported increased energetics of movement and fatigue in ambulatory children with CP. What this paper adds Skeletal muscle mitochondrial electron transport chain enzymatic activity is reduced in independently ambulatory children with cerebral palsy (CP). Mitochondrial content appears to be similar between children with CP and typically developing children.
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