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Zellweger Syndrome |
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Zellweger syndrome is a rare, congenital disorder (present at birth), characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic substances) in the cells of the liver, kidneys, and brain. It is characterized by an individual's inability to beta-oxidize very-long chain fatty acids in the peroxisomes of the cell, due to a genetic disorder in the PEX2 gene. ...
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Zellweger Syndrome Other1-2 of 2
Zellweger Syndrome
... What is Zellweger Syndrome? Zellweger syndrome is a rare, congenital (present at birth) disorder characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic su...
Source: Cleveland Clinic
Zellweger Syndrome Information Page ... Zellweger syndrome is a rare, congenital (present at birth) disorder characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic substances) in the cells of th...
Source: National Institute of Neurological Disorders and Stroke
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Zellweger Syndrome Articles
- Zellweger Syndrome Information Page
... Zellweger syndrome is a rare, congenital (present at birth) disorder characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic substances) in the cells of th...
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