An inherited form of anemia caused by faulty synthesis of hemoglobin.
Отсутствуют примеры синонимов
1 Derangements in phosphate and calcium homeostasis are common in patients with beta- thalassemia .
2 Beta- thalassemia is a genetic disorder caused by mutations in the beta-globin gene.
3 The primers for determination of different subsets of alpha thalassemia deletions were included.
4 It is postulated that thalassemia minor may be a risk factor for osteoporosis.
5 SF could not reliably predict iron overload in all thalassemia patients.
6 A total of 156 samples were analyzed for alpha thalassemia mutations.
7 Eleven index patients were multitransfused because of thalassemia major.
8 This is a generally uncommon event in thalassemia intermedia.
9 De Salvatore has thalassemia , a blood disorder that requires transfusions every two to three weeks.
10 Results: No cases of beta thalassemia were diagnosed in this cohort of French patients with PXE.
11 The beta thalassemia gene possessed a splicing site mutation known to create a beta thalassemia phenotype.
12 The inherited hemoglobin disorders sickle cell disease and thalassemia are the most common monogenetic disorders worldwide.
13 Beta- thalassemia and sickle cell anemia are two of the most common diseases related to the hemoglobin protein.
14 We attempted to determine the incidence of beta thalassemia in a cohort of French patients with PXE.
15 They both suffer from thalassemia and their condition has been exacerbated by the lack of rich food.
16 Splice-site mutations in the beta-globin gene can lead to aberrant transcripts and decreased functional beta-globin, causing beta- thalassemia .
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Translations for thalassemia