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SCAD

Mitochondrial Disease Types

SCAD

Long Name: Short-Chain Acyl-CoA Dehydrogenase Deficiency

Symptoms: Failure to thrive, developmental delay, and hypoglycemia

Cause: Autosomal recessive

Treatment: See Beta-oxidation Defects

Links: https://rarediseases.info.nih.gov/diseases/4822/short-chain-acyl-coa-dehydrogenase-deficiency

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Mission of UMDF

To promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and to provide support to affected individuals and families.

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