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This is the American ICD-10-CM version of D57.2 - other international versions of ICD-10 D57.2 may differ. One of the sickle cell disorders characterized by the presence of both hemoglobin s and hemoglobin c. It is similar to, but less severe than sickle cell anemia.
- D57.40
D57.40 is a billable/specific ICD-10-CM code that can be...
- D57.40
Haemoglobin SC disease is a sickling disorder which results from the co-inheritance of two abnormal ß globin genes, haemoglobin S and haemoglobin C (ß s ß c). It is characterised by the presence of SC poikilocytes, abnormally contracted cells which resemble sickle cells but which have straight edges or are branched.
4 Οκτ 2022 · Sickle cell disease (SCD) is an inherited group of disorders characterized by the presence of hemoglobin S (Hb S), either from homozygosity for the sickle mutation (Hb SS) or compound heterozygosity with another beta globin variant (eg, sickle-beta thalassemia, Hb SC disease).
Hemoglobin S-C disease is suspected in patients whose clinical features suggest sickle cell disease or whose red blood cells demonstrate sickling. Stained blood smears show target cells, spherocytes, and rarely sickle cells or oat-shaped cells.
Like sickle cell anemia, the hematological and clinical features of HbSC disease are heterogeneous, but all of the complications that make sickle cell anemia notorious can be present; some even appear more often in HbSC disease. HbC and HbC Disease. Origins, Selection, and Distribution of HbC.
Hemoglobin SC Disease, also known as Sickle Cell Disease-SC, is a combination of hemoglobin S and hemoglobin C. It is characterized by mild anemia, hemolytic features, the presence of target cells in the blood smear, and a positive sickle cell preparation.
Hemoglobin (Hb)-SC disease results from a combination of sickle cell trait coinherited with the β-globin C trait. This results in a sickling condition with generally milder hemolytic anemia and less frequent acute and chronic complications.
