| sickle cell t. |
the condition, usually asymptomatic, caused by heterozygosity for hemoglobin S.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sickle cell–hemoglobin C d. |
a genetically determined anemia in which the erythrocytes contain both hemoglobin S and hemoglobin C; symptoms are similar to but less severe than those of sickle cell anemia and may include abdominal and skeletal pain, splenomegaly, splenic infarction, and infarctions or deformities of bone. Called also hemoglobin SC d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sickle cell–hemoglobin D d. |
a genetically determined anemia in which the erythrocytes contain both hemoglobin S and hemoglobin D, with symptoms like those of mild sickle cell anemia. Called also hemoglobin SD d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sickle cell–t. |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sickle cell–thalassemia d. |
any of several hereditary anemias involving simultaneous heterozygosity for hemoglobin S and a thalassemia gene; symptoms resemble those of sickle cell anemia. Called also microdrepanocytosis, microdrepanocytic d., hemoglobin S–thalassemia, sickle cell–thalassemia, and thalassemia–sickle cell d..
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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