Congenital hemolytic anemia

Congenital hemolytic anemia
Other names	Hereditary hemolytic anemia
Specialty	Hematology

Congenital 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
- Hereditary spherocytosis
- Hereditary elliptocytosis
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 abnormalities as well, but rather encompassing defects of glycolysis in the erythrocyte.[2]
- Glucose-6-phosphate dehydrogenase deficiency (G6PD or favism)
- Pyruvate kinase deficiency
- Aldolase A deficiency
Hemoglobinopathies[3]/genetic conditions of hemoglobin
- Sickle cell anemia
- Congenital dyserythropoietic anemia

Rahman SA, Jamal CY (June 2002). "Congenital hemolytic anemia in Bangladesh: types and clinical manifestations". Indian Pediatr. 39 (6): 574–7. PMID 12084953.
medconditions.net > Hemolytic Congenital, Nonspherocytic Anemia Definition Archived 2016-09-19 at the Wayback Machine Retrieved April 15, 2011
Shah A (November 2004). "Hemoglobinopathies and other congenital hemolytic anemia". Indian J Med Sci. 58 (11): 490–3. PMID 15567909.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.