| 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...
|
|---|---|
| sickle cell–t. |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| 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...
|
| sickle s. |
a scaler that removes tenacious supragingival or subgingival deposits; it has a sickle-like blade with flattened sides and a trapezoidal cross section.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| sicklemia |
sickle cell anemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|