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1 серповидно-клеточная гемоглобинопатия
Большой русско-английский медицинский словарь > серповидно-клеточная гемоглобинопатия
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2 серповидно-клеточная гемоглобинопатия
Medicine: sickle-cell hemoglobinopathyУниверсальный русско-английский словарь > серповидно-клеточная гемоглобинопатия
См. также в других словарях:
Sickle-cell disease — This article is about the disease itself. For the genetic transmission of sickle cell disease and its carrier state, see sickle cell trait. Sickle cell disease Classification and external resources Normal and sickle shaped red blood cells ICD 10 … Wikipedia
sickle cell anemia — Pathol. a chronic hereditary blood disease, occurring primarily among Africans or persons of African descent, in which abnormal hemoglobin causes red blood cells to become sickle shaped and nonfunctional, characterized by enlarged spleen, chronic … Universalium
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… … Universalium
sickle cell anemia — Synonyms and related words: Christmas disease, Hand Schuller Christian disease, Hartnup disease, Letterer Siwe syndrome, Werdnig Hoffmann disease, achromatic vision, acute leukemia, albinism, anemia, angiohemophilia, aplastic anemia, chronic… … Moby Thesaurus
Hemoglobinopathy — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 19674 ICD10 = ICD10|D|58|2|d|55 ICD9 = ICD9|282.7 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D006453 Hemoglobinopathy is a kind of genetic defect that results in… … Wikipedia
hemoglobinopathy — Any of a group of disorders caused by genetic abnormality of the hemoglobin molecule. The most prominent types are sickle cell anemia and thalassemia, a set of disorders whose symptoms range from none to fatal anemia. * * * also spelled… … Universalium
hemoglobinopathy — A disorder or disease caused by or associated with the presence of abnormal hemoglobins in the blood, e.g., sickle cell disease, hemoglobin C, D, E, H, or I disorders. Occasionally, combinations of abnormal hemoglobins are seen in… … Medical dictionary
hemoglobinopathy — noun (plural thies) Date: 1957 a blood disorder (as sickle cell anemia) caused by a genetically determined change in the molecular structure of hemoglobin … New Collegiate Dictionary
Pure red cell aplasia — Classification and external resources ICD 10 D60 ICD 9 284.8 … Wikipedia
Hemoglobin — Hemoglobin, human, adult (heterotetramer, (αβ)2) Structure of human hemoglobin. The protein s α and β subunits are in red and blue, and the iron containing heme groups in green. Fro … Wikipedia
Thalassemia — Classification and external resources ICD 10 D56 ICD 9 282.4 … Wikipedia