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Congenital Nonspherocytic Hemolytic Anemia 1
A congenital nonspherocytic hemolytic anemia that is caused by mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia.
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When to seek help
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Overview
A congenital nonspherocytic hemolytic anemia that is caused by mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia.
Resources
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