| hemoglobin S–t. |
sickle cell–thalassemia disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin SC d. |
sickle cell–hemoglobin C d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin SD d. |
sickle cell–hemoglobin D d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| 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:
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| 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.
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