Congenital hemolytic anemia

Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[1]

Congenital hemolytic anemia
Other names	Hereditary hemolytic anemia
Specialty	Hematology

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

• • Thalassemia

See also

• Hematopoietic ulcer
• List of circulatory system conditions

References

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

External links

Classification	D ICD-10: D55-D58 ICD-9-CM: 282 MeSH: D000745