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3-Hydroxyisobutryl-CoA Hydrolase Deficiency
An amino acid metabolic disorder characterized by severely delayed psychomotor development, neurodegeneration, increased lactic acid, and brain lesions in the basal ganglia that is caused by homozygous or compound hetero
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When to seek help
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Overview
An amino acid metabolic disorder characterized by severely delayed psychomotor development, neurodegeneration, increased lactic acid, and brain lesions in the basal ganglia that is caused by homozygous or compound hetero
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.