Congenital hemolytic anemia
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| Congenital hemolytic anemia | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | D55-D58 |
| ICD-9-CM | 282 |
| Patient UK | Congenital hemolytic anemia |
| MeSH | D000745 |
Congenital hemolytic anemia (or hereditary hemolytic anemia) refers to hemolytic anemia which is primarily due to congenital disorders.[1]
Types
Basically classified by causative mechanism, types of congenital hemolytic anemia include:
- Genetic conditions of RBC Membrane
- Genetic conditions of RBC metabolism (enzyme defects). This group is sometimes called congenital nonspherocytic (hemolytic) anemia, which is a term for a congenital hemolytic anemia without spherocytosis, and usually excluding hemoglobin abdormalities as well, but rather encompassing defects of glycolysis in the erythrocyte.[2]
- Hemoglobinopathies[3]/genetic conditions of hemoglobin
See also
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ medconditions.net > Hemolytic Congenital, Nonspherocytic Anemia Definition Retrieved April 15, 2011
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
