Congenital hemolytic anemia: Difference between revisions
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'''Congenital hemolytic anemia''' (or '''hereditary hemolytic anemia''') refers to [[hemolytic anemia]] which is primarily due to [[congenital disorder]]s.<ref name="pmid12084953">{{cite journal |author=Rahman SA, Jamal CY |title=Congenital hemolytic anemia in Bangladesh: types and clinical manifestations |journal=Indian Pediatr |volume=39 |issue=6 |pages=574–7 |year=2002 |month=June |pmid=12084953 |doi= |url=}}</ref> | '''Congenital hemolytic anemia''' (or '''hereditary hemolytic anemia''') refers to [[hemolytic anemia]] which is primarily due to [[congenital disorder]]s.<ref name="pmid12084953">{{cite journal |author=Rahman SA, Jamal CY |title=Congenital hemolytic anemia in Bangladesh: types and clinical manifestations |journal=Indian Pediatr |volume=39 |issue=6 |pages=574–7 |year=2002 |month=June |pmid=12084953 |doi= |url=}}</ref> | ||
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Revision as of 00:10, 9 August 2012
| Congenital hemolytic anemia | |
| ICD-10 | D55-D58 |
|---|---|
| ICD-9 | 282 |
| MeSH | D000745 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Congenital hemolytic anemia (or hereditary hemolytic anemia) refers to hemolytic anemia which is primarily due to congenital disorders.[1]
Types include:
- Genetic conditions of RBC Membrane
- Genetic conditions of RBC metabolism (enzyme defects)
- Glucose-6-phosphate dehydrogenase deficiency (G6PD or favism)
- Pyruvate kinase deficiency
- Hemoglobinopathies[2]/genetic conditions of hemoglobin
References
- ↑ Rahman SA, Jamal CY (2002). "Congenital hemolytic anemia in Bangladesh: types and clinical manifestations". Indian Pediatr. 39 (6): 574–7. PMID 12084953. Unknown parameter
|month=ignored (help) - ↑ Shah A (2004). "Hemoglobinopathies and other congenital hemolytic anemia". Indian J Med Sci. 58 (11): 490–3. PMID 15567909. Unknown parameter
|month=ignored (help)