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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...
- 2025 ICD-10-CM Diagnosis Code D57.20
Clinical Information. One of the sickle cell disorders...
- D57.40
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.
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.
Clinical Information. 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. ICD-10-CM D57.20 is grouped within Diagnostic Related Group (s) (MS-DRG v42.0): 811 Red blood cell disorders with mcc. 812 Red blood cell disorders without mcc.
Hemoglobin C, S-C, and E diseases are inherited conditions characterized by gene mutations that affect the hemoglobin (the protein that carries oxygen) in red blood cells. These red blood cells are destroyed more quickly than others, resulting in chronic anemia.
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).
Clinical features. Hb SC disease usually results in a milder form of SCD, but it can be severe in some cases. Growth and development are delayed compared with normal children. Unlike Hb SS, Hb SC usually does not produce significant symptoms until the teenage years.
