Zellweger Syndrome is a rare hereditary disorder affecting infants. It is characterized by reduction or absence of peroxisomes in the cells of the liver, kidneys, and brain.
Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics.
Offers alternate names, a general discussion and resources.
Clinical information on this disorder characterized by an individual's inability to beta-oxidize very-long chain fatty acids.
Provides support to families who are affected by this disorder. Includes information on Zellweger and related disorders, research, message boards and chat.
Information page compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
Thanks to DMOZ, which built a great web directory for nearly two decades and freely shared it with the web. About us