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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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.
Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics.
Clinical information on this disorder characterized by an individual's inability to beta-oxidize very-long chain fatty acids.
Offers alternate names, a general discussion and resources.
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Last update:
March 19, 2018 at 11:15:07 UTC
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Regional: North America: United States: Nebraska: Localities: H: Hyannis
- Recently edited by cherel
- Recently edited by cherel