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Encyclopedia > Acatalasemia

Acatalasemia is a genetic deficiency of erythrocyte catalase. It is inherited as an autosomal recessive trait. link title Catalase Catalase (human erythrocyte catalase: PDB 1DGF, EC 1. ...


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Acatalasemia (60 words)
Acatalasemia is a congenital disorder resulting from a deficiency in erythrocyte catalase, an enzyme responsible for the breakdown of hydrogen peroxide.
The disorder is very rare in the general population with an estimated prevalence of 1 in 31250.
The disorder is usually asymptomatic but may be associated with oral ulcerations and gangrene, or diabetes mellitus and atherosclerosis in certain populations.
Acatalasemia - Wikipedia, the free encyclopedia (56 words)
Acatalasemia is a genetic deficiency of erythrocyte catalase.
Acatalasemia is inherited in an autosomal recessive fashion.
This page was last modified 04:23, 8 August 2006.
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