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Metabolic Disorders as related to Acrodysostosis


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Progeria 

 

Progeria is an extremely rare genetic condition which causes physical changes that resemble greatly accelerated aging in sufferers. It is an autosomal recessive condition that affects around 1 in 4-8 million newborns. Currently, there are approximately 35 known cases in the world with no known cure. Most children with the disease die around 13 years of age.

Acrodysostosis also known as Arkless-Graham syndrome or Maroteaux-Malamut syndrome is a rare congenital malformation syndrome which involves ...


Metabolic Disorders as related to Acrodysostosis


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November 27, 2009


Page Updated: January 17, 2009
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