D2I2.
genetic

Zellweger syndrome

Zellweger is a rare disorder characterized by the reduction or absence of functional peroxisomes in the cells of an individual. It is one of a family of disorders called Zellweger disorders which are leukodystrophies. Zellweger syndrome is named after Hans Zellweger (1909–1990), a Swiss-American pediatrician, a professor of pediatrics and at the University of Iowa who researched this disorder.

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Complications

  • · and distress.
Plain-language summary adapted from Wikipedia. Not medical advice.