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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.
Sickle Cell Retinopathy is recognized by the following codes as per the International Classification of Diseases (ICD) nomenclature: ICD-10-CM Diagnosis Code H36. Description Synonyms. Proliferative retinopathy due to sickle cell disease. Retinal dystrophy due to systemic disorder.
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 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.
16 Απρ 2020 · Hemoglobin levels in children with HbSβ + thalassemia vary. The range is from hemoglobin levels of 7 g/dL to values within the normal range. The low hemoglobin levels are accompanied by magnitudes of hemolysis markers similar to those seen in children with HbSS.
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).
