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Disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs; the clinical expression of homozygosity for hemoglobin s. Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells.
- D57.00
ICD 10 code for Hb-SS disease with crisis, unspecified. Get...
- D57.00
ICD 10 code for Hb-SS disease with crisis, unspecified. Get free rules, notes, crosswalks, synonyms, history for ICD-10 code D57.00.
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.
26 Φεβ 2024 · Some children and adults with hemoglobin SC disease have chronic pain resulting from ulcers and bone and joint damage. Swollen feet and hands. The lack of blood flow in the body can cause...
People with this disease have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape. Signs and symptoms of sickle cell disease usually begin in early childhood.
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.
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.
