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Causes Of Zellweger Syndrome

Zellweger Syndrome is one of types of peroxisomal metabolic disorders. It is an inherited syndrome. It is caused due to mutations in the gene located in the 12th chromosome. Perioxisomes are structures that are present in the cells of the liver, brain and kidneys. They are responsible for removing any toxic material from the cells. If a person suffers from Zellweger syndrome, there is a reduction or complete cessation of the production of perioxisomes, and this can adversely affect the body.More...

Facts On Zellweger Syndrome

Zellweger syndrome is a genetic disorder that is inherited. The disorder is present at birth, and the infant usually succumbs to it within the first year of its birth. The syndrome causes a reduction or complete lack of certain cytoplasmic organelles known as perioxisomes. These organelles help to detoxify the cells and also contain certain important enzymes that are required for the different chemical processes that go on in the cells.More...

 

How Zellweger Syndrome Effect On Cells ?

Zellweger syndrome is an inherited genetic disorder that adversely affects the liver, brain and kidneys. If both parents have the specific gene for the syndrome, then there is a twenty-five percent chance that the child will inherit the syndrome. Zellweger syndrome is present at birth, and is usually diagnosed based on the characteristic appearance of the face and head.More...