| hemoglobin E d. |
the state of being homozygous for hemoglobin E; many patients are asymptomatic, but others have mild hemolytic anemia, usually without splenomegaly, and increased numbers of normochromic target cells in the peripheral blood.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| hemoglobin E–t. |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hemoglobin E–thalassemia d. |
a hereditary condition involving simultaneous heterozygosity for hemoglobin E and thalassemia, manifested by mild hemolytic anemia and persistent splenomegaly; called also hemoglobin E–thalassemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hemoglobin E disease |
A genetic variant of hemoglobin that produces a mild form of hemolytic anemia. It is primarily in persons of Southeast Asian origin, in whom it may provide protection against falciparum malaria.
출처:
|