sickle cell

الإنجليزية - التركية

تعريف sickle cell في الإنجليزية التركية القاموس.: (Biyokimya) orak göze; orak hücre
sickle cell anemia: orak hücre anemisi
sickle cell anemia: orak hücreli anemi
sickle cell disease: (Tıp, İlaç) Orak hücre hastalığı
sickle-cell: Orak hücreli

الإنجليزية - الإنجليزية

تعريف sickle cell في الإنجليزية الإنجليزية القاموس.: (Tıp, İlaç) An abnormal red blood cell that has a crescent shape and an abnormal form of hemoglobin; An abnormal, crescent-shaped red blood cell that results from a single change in the amino acid sequence of the cell's hemoglobin, which causes the cell to contort, especially under low-oxygen conditions
sickle cell anemia: A chronic, usually fatal anemia marked by sickle-shaped red blood cells, occurring almost exclusively in Black people of Africa or of African descent, and characterized by episodic pain in the joints, fever, leg ulcers, and jaundice. The disease occurs in individuals who are homozygous for a mutant hemoglobin gene. Also called sickle cell disease
sickle cell anemia: (Medicine) hereditary disease characterized by anemia resulting from defective hemoglobin production (causes deformed red blood cells, oxygen deficiency, and circulatory problems)
sickle cell trait: A hereditary condition, usually harmless and without symptoms, in which an individual carries only one mutated hemoglobin gene for sickle cell anemia
sickle-cell anaemia: A disease characterized by sickle-shaped red blood cells
sickle-cell anemia: A disease characterized by sickle-shaped red blood cells
sickle-cell disease: A disease characterized by sickle-shaped red blood cells
sickle-cell anaemia: sickle-cell anaemia in AM, use sickle-cell anemia Sickle-cell anaemia is an inherited illness in which the red blood cells become curved, causing a number of health problems. sickle-cell anemia a serious illness that mainly affects black people, in which the blood cells change shape, causing weakness and fever
sickle-cell anemia: Blood disorder (see hemoglobinopathy) seen mainly in persons of Sub-Saharan African ancestry and their descendants and in those from the Middle East, the Mediterranean area, and India. About 1 in 400 blacks worldwide has the disease, caused by inheriting two copies of a recessive gene that makes those with one copy (about 1 in 12 blacks worldwide) resistant to malaria. The gene specifies a variant hemoglobin (hemoglobin S or Hb S) that distorts red blood cells (erythrocytes) into a rigid sickle shape. The cells become clogged in capillaries, damaging or destroying various tissues. Symptoms include chronic anemia, shortness of breath, fever, and episodic "crises" (severe pain in the abdomen, bones, or muscles). Hydroxyurea treatment triggers production of fetal hemoglobin (Hb F), which does not sickle, greatly lessening severity of crises and increasing life expectancy, previously about 45 years
sickle-cell anemia: a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape