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Differential Diagnosis For Hallervorden-Spatz disease - Causes, Family history/Enzyme defect

List of current finding(s):

Hallervorden-Spatz disease - Causes
Family history/Enzyme defect
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Metabolic, Storage Disorders: LCHAD/Long chain OH-CoA dehydrogenase def; MCAD/Medium chain OH-CoA Dehydrogenase def; VLCHAD/Very Long chain OH-CoA dehydrogenase def; Alkaptonuria/Ochronosis; Galactosemia
Hereditary, Familial, Genetic Disorders: Hallervorden-Spatz disease (PKAN/NBIA)

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