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What is hemoglobin SC disease?
Persons with hemoglobin SC disease inherit a hemoglobin S (sickle) gene from one parent and a hemoglobin C gene from the other parent. Hemoglobin SC disease is a form of sickle cell disease.
Hemoglobin SC disease (similar in symptoms to sickle-cell anemia)
Hemolytic anemia due to G6PD deficiency
Hereditary elliptocytosis
Hereditary ovalocytosis
Hereditary spherocytosis
Idiopathic autoimmune hemolytic anemia
Malaria ...
Hemoglobin SC disease
It is similar to sickle cell anemia, but usually less severe.
Anxiety, Deficiency, Factor X, Degeneration, Familial Spinocerebellar, Disorders, Phobic, Drugs, Street, Factor VIII Deficiency, Fibromatoses, Genital Tuberculosis, Male, Glutamate, Hemoglobin SC Diseases, Hydrochloride, Lucanthone, Immunoglobulins, ...
Hemoglobin SC disease
Hemoglobin sickle beta-thalassemiaEach of these can cause sickle pain episodes and complications, but some are more common than others.
Sickle cell anemia is one of 3 common types of sickle cell disease in the US. The other 2 types are called hemoglobin SC disease and sickle thalassemia. The 3 conditions differ in the types and amounts of abnormal hemoglobin in the blood.
 See also: Anemia, Infections, Symptom, Thalassemia, Prevention
  
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