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21 Σεπ 2018 · Hemoglobin C disease (Hb CC) is a mild disorder that generally does not cause any symptoms and is associated with a normal life expectancy. Affected individuals exhibit normal growth and...
29 Μαΐ 2023 · Persons with hemoglobin C trait (Hb AC) are phenotypically normal and generally do not show any symptoms while persons with hemoglobin C disease (Hb CC) may present with mild chronic hemolysis, splenomegaly, and jaundice.
30 Νοε 2021 · Hemoglobin C disease is a blood disorder that can cause fatigue, weakness, and anemia. It occurs when a person inherits two copies of hemoglobin C genes from their parents.
Hemoglobin C disease is a hemoglobinopathy that causes symptoms of a hemolytic anemia. (See also Overview of Hemolytic Anemia .) The prevalence of detectable hemoglobin (Hb) C in people in the United States with African ancestry is approximately 2 to 3%.
Hemoglobin C trait is a condition that affects the red blood cells. Your red blood cells contain hemoglobin, which carries oxygen from the lungs to all parts of your body.
Hemoglobin SC disease is caused by a copy of hemoglobin S gene inherited from one parent, and a hemoglobin C gene inherited from the other. The hemoglobin C molecule disturbs the red-cell metabolism only slightly.
Hemoglobin C disease is a hemoglobinopathy that causes symptoms of a hemolytic anemia. (See also Overview of Hemolytic Anemia .) The prevalence of detectable hemoglobin (Hb) C in people in the US with African ancestry is about 2 to 3%. Patients who are heterozygotes are asymptomatic.
