fetal hemoglobin胎儿血红蛋白 synthesis合成 chromosome16 16号染色体 mutation(基因)突变 mutated gene突变基因 gene deletion基因缺失 autosomal recessive pattern常染色体隐性遗传方式 defective异常的,有问题的 silent carrier无症状携带者 Alpha-thalassemia minor轻度α-地中海贫血 mild轻度 moderate中度 severe重度 cis-del...
minor ___→___ menor. English-Spanish Medical Dictionary © Farlex 2012 thalassemia ntalasemia English-Spanish/Spanish-English Medical Dictionary Copyright © 2006 by The McGraw-Hill Companies, Inc. All rights reserved. Want to thank TFD for its existence?Tell a friend about us, add a link...
beta thalassemia major are almost never symptomatic at birth because o the presence o HbF, but symptoms begin to develop by six months o age. I the synthesis SORT: KEY RECOMMENDATIONS FOR PRACTICE Clinical recommendation Evidence rating Re erences Persons with anemia rom thalassemia...
These patients are sometimes referred to as “silent carriers” because there are no clinical symptoms but mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH) may be slightly decreased. These individuals are diagnosed by deduction only when they have children with a thalassemia trait...
3.Andalphathalassemia is caused by mutations in thealphagenes, most commonly a gene deletion. 而α地中海贫血是由α基因变异引起的,常见的原因是基因缺失。 「Osmosis-遗传」评价该例句:好评差评指正 美丽新世界 4.They wereAlphas, of course, but evenAlphashave been well conditioned. ...
Between these extremes, alpha thalassemia intermedia, or HbH disease, is generally thought to be a mild disorder, although its clinical expression can range from no symptoms to hemolysis with severe anemia, requiring intermittent transfusions, and even to fatal hydrops fetalis (Chui et al. 2003...
thalassemia [‚thal·ə′sē·mē·ə] (medicine) A hereditary form of hemolytic anemia resulting from a defective synthesis of hemoglobin: thalassemia major is the homozygous state accompanied by clinical illness, and thalassemia minor is the heterozygous state and may not have evident clinical...
(--/αTα). Whereas clinical phenotypes of the former are usually homogenously mild to moderate, those of the latter can be diverse. As HbH disease is particularly prevalent in Southeast Asia and some parts of the Mediterranean region, where β-thalassemia is also prevalent, affected patients ...
Bordbar, E.; Taghipour, M.; Zucconi, B.E. Reliability of Different RBC Indices and Formulas in Discriminating between β-Thalassemia Minor and other Microcytic Hypochromic Anemia.Mediterr. J. Hematol. Infect. Dis.2015,7, e2015022. [Google Scholar] [CrossRef] [PubMed] ...