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The Fabry Disease

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Classification is a hereditary disorder, caused by the lack of alphagalactosidase A. It is an x-linked recessive inheritance. Therefore it is the females that carry it. The ones who are mostly affected by this disease are the males. Female carriers, though, may develop angiokeratomas and may h ....

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....examination. Prenatal diagnosis by way of Amniocentesis or Chronic Villus Sampling is also available. Prognosis People affected by this disorder usually dies by the age of 40-50 from kidney failure or cerbovascular complications. Treatment There is only treatment to relieve the pains of the symptoms. Researchers are working towards the possibility of replacing the enzyme. Bibliography The Encyclopedia of Genetic Disorder and Birth Defects, By James Wynbrandt and Mark D. Ludman, M.D., F....
Number of words: 331 Approximate pages: 2

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