| 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:
|
|---|---|
| hemoglobin M disorder |
A genetic variant of hemoglobin that causes cyanosis and methemoglobinemia. The iron in this type of hemoglobin is in the ferric (Fe3+) state and cannot combine with oxygen.
출처:
|
| hemoglobin S disease |
A genetic variant of hemoglobin that causes sickle cell trait in heterozygotes, and sickle cell disease in hemozygotes. It is common, esp. in persons of African ancestry in whom sickle cell trait is found in 8?10% of the pop
출처:
|
| hemoglobin SC disease |
A disease of persons who have inherited two abnormal forms of hemoglobin, S and C. Affected persons may have vaso-occlusive crises similar to those seen in sickle cell anemia, with bony and visceral infarcts.
출처:
|
| hemoglobin |
A protein complex found in red blood cells, composed of two proteins (alpha and beta) that bind molecular oxygen for transport through out the body.
출처: www.cwu.edu/~chem/courses/chem388488f00/mcclung/mc...
|