DMOZ Internet Directory : Health : Conditions_and_Diseases : Nutritional_and_Metabolic_Disorders : Inherited : Zellweger

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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.

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NORD: Zellweger Syndrome - Offers alternate names, a general discussion and resources. Zellweger Syndrome - Information page compiled by NINDS, the National Institute of Neurological Disorders and Stroke. Zellweger Baby Support Network - Provides support to families who are affected by this disorder. Includes information on Zellweger and related disorders, research, message boards and chat. GeneReviews: Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum - Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics. Online Mendelian Inheritance in Man: Zellweger Syndome - Clinical information on this disorder characterized by an individual's inability to beta-oxidize very-long chain fatty acids.

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