ACAD8 deficiency: An extremely rare metabolic disorder where the body is unable to metabolize certain proteins properly. More specifically, an insufficient level of the enzyme (isobutyryl-coenzyme A dehydrogenase) needed to metabolize the amino acid valine. The onset and severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of ACAD8 deficiency is available below.
See full list of 13 symptoms of ACAD8 deficiency
Review possible medical complications related to ACAD8 deficiency:
Read more about causes of ACAD8 deficiency
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Prognosis for ACAD8 deficiency: Early diagnosis and treatment can significantly improve the prognosis.
More about prognosis of ACAD8 deficiency
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