Article
Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype.
Molecular genetics and metabolism - 1 Nov 2021
Enns Gregory M, Ammous Zineb, Himes Ryan W, Nogueira Janaina, Palle Sirish, Sullivan Meghan, Ramirez Charina
Abstract excerpt
Peroxisome Biogenesis Disorders-Zellweger spectrum disorder (PBD-ZSD) is a rare, autosomal recessive peroxisome biogenesis disorder that presents with variable symptoms. In patients with PBD-ZSD, pathogenic variants in the PEX family of genes disrupt normal peroxisomal function, impairing α- and β-oxidation of very-long-chain fatty acids and synthesis of bile acids, resulting in increased levels of toxic bile...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
