PedAM
Pediatric Disease Annotations & Medicines
| Disease | thalassemia |
| Phenotype | C0002878|hemolytic anemia |
| Sentences | 6 |
| PubMedID- 22475299 | Autoimmune hemolytic anemia in patients with beta-thalassemia major. |
| PubMedID- 21883965 | This hb disorder can form a compound heterozygous state with the beta-thalassemia gene, leading to life-threatening hereditary hemolytic anemia, hbe/beta-thalassemia. |
| PubMedID- 24348256 | Dulinska et al., demonstrated that the young's modulus in erythrocytes from patients with hemolytic anemia due to hereditary spherocytosis, thalassemia, or glucose-6-phophate dehydrogenase deficiency is 1.5 to 3.5-fold greater than the young's modulus of normal erythrocytes [48]. |
| PubMedID- 23402775 | thalassemia major presents with chronic hemolytic anemia that requires regular red blood cell transfusions within the first year of life. |
| PubMedID- 24456650 | Heterozygosity for a large duplication of the complete α-globin gene cluster, including the upstream regulatory element hs-40, was identified in a β-thalassemia carrier with severe hemolytic anemia (figure 4b). |
| PubMedID- 25883429 | Severe hemolytic anemia in beta-thalassemia major and beta-thalassemias/hbe (beta-tm) patients requires giving blood transfusions. |
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