Congenital hemolytic anemia: Difference between revisions
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==Classification== | ==Classification== | ||
Types include: | Types include: | ||
*Genetic conditions of RBC | *Genetic conditions of the RBC membrane: | ||
**[[Hereditary spherocytosis]] | **[[Hereditary spherocytosis]] | ||
**[[Hereditary elliptocytosis]] | **[[Hereditary elliptocytosis]] | ||
*Genetic conditions of RBC metabolism ([[enzyme]] defects) | *Genetic conditions of RBC metabolism ([[enzyme]] defects): | ||
**[[Glucose-6-phosphate dehydrogenase deficiency]] (G6PD or favism) | **[[Glucose-6-phosphate dehydrogenase deficiency]] (G6PD or favism) | ||
**[[Pyruvate kinase deficiency]] | **[[Pyruvate kinase deficiency]] | ||
*[[Hemoglobinopathies]]<ref name="pmid15567909">{{cite journal |author=Shah A |title=Hemoglobinopathies and other congenital hemolytic anemia |journal=Indian J Med Sci |volume=58 |issue=11 |pages=490–3 |year=2004 |month=November |pmid=15567909 |doi= |url=}}</ref>/genetic conditions of hemoglobin | *[[Hemoglobinopathies]]<ref name="pmid15567909">{{cite journal |author=Shah A |title=Hemoglobinopathies and other congenital hemolytic anemia |journal=Indian J Med Sci |volume=58 |issue=11 |pages=490–3 |year=2004 |month=November |pmid=15567909 |doi= |url=}}</ref>/genetic conditions of [[hemoglobin]]: | ||
**[[Sickle cell anemia]] | **[[Sickle cell anemia]] | ||
**[[Thalassaemia]] | **[[Thalassaemia]] | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 13:57, 3 June 2013
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Hereditary hemolytic anemia
Overview
Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[1]
Classification
Types include:
- Genetic conditions of the 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)