| hemoglobin C d. |
the state of being homozygous for hemoglobin C, characterized by splenomegaly, mild to moderate hemolytic anemia, recurrent jaundice, and increased numbers of target cells and reticulocytes in the peripheral blood.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin C t. |
the heterozygous state for hemoglobin C; it is asymptomatic although individuals have increased target cells in the blood. See also hemoglobin C–thalassemia disease, under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin C–t. |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin C–thalassemia d. |
a hereditary disorder involving simultaneous heterozygosity for hemoglobin C and thalassemia, manifested by mild hemolytic anemia and persistent splenomegaly; called also hemoglobin C–thalassemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin c. |
a granular cast that contains hemoglobin, such as in tubular bleeding or glomerulopathy.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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