Zellweger Syndrome

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Zellweger Syndrome is a genetic disorder characterized by the lack of functional peroxisomes in cells.

It is an autosomal recessive disorder that is caused by a mutation in the PEX genes. Characteristic findings include hypotonia, hepatomegaly, seizures, and early death.

Find Zellweger Syndrome and other Peroximal Disorders among Pixorize's visual mnemonics for the USMLE Step 1 and NBME Shelf Exams.