| sickle cell c. |
a broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vaso-occlusive crisis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sickle cell d. |
any of the diseases associated with the presence of hemoglobin S and sickle cells, including sickle cell anemia, sickle cell–hemoglobin C disease, sickle cell–hemoglobin D disease, and sickle cell–thalassemia disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sickle cell n. |
chronic kidney pathology seen with sickle cell disease, including microangiopathy with capillary obstruction, dilated or obliterated vasa recta, enlarged glomeruli, interstitial fibrosis, and an increased glomerular filtration rate.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| 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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