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SCHAD

Mitochondrial Disease Types

SCHAD

Short Chain 3-hydroxyacyl CoA Dehydrogenase Deficiency

Symptoms: Encephalopathy and possibly liver disease or cardiomyopathy

Cause: Autosomal recessive

Treatment: See Beta-oxidation Defects

Links: https://rarediseases.info.nih.gov/diseases/9870/3-alpha-hydroxyacyl-coa-dehydrogenase-deficiency

Last Updated:  Dec 26, 2022 @ 4:13 pm

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