Keywords

#aldolase_a_deficiency

Aldolase A deficiency

Medical condition

Aldolase A deficiency is an autosomal recessive metabolic disorder resulting in a deficiency of the enzyme aldolase A; the enzyme is found predominantly in red blood cells and muscle tissue. The deficiency may lead to hemolytic anaemia as well as myopathy associated with exercise intolerance and rhabdomyolysis in some cases.

Mon 14th

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Aldolase A deficiency Aldolase A Congenital hemolytic anemia Hereditary fructose intolerance Glycogen storage disease Inborn errors of carbohydrate metabolism List of diseases (A) Aldolase B Glycogen storage disease type 0 Phosphofructokinase deficiency
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