ABMGG Medical Biochemical Genetics
Peroxisomal DisordersEnglish
Exam overviewPractice session
A neonate presents with profound hypotonia, seizures, hepatomegaly, dysmorphic features (high forehead, large fontanelle), and bilateral cataracts. Plasma very long chain fatty acids show elevated C26:0 and elevated C26:0/C22:0 ratio. What is the diagnosis?
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