PedAM
Pediatric Disease Annotations & Medicines
| Disease | hemolytic anemia |
| Phenotype | C0039730|thalassemia |
| Sentences | 6 |
| 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- 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- 22475299 | Autoimmune hemolytic anemia in patients with beta-thalassemia major. |
| PubMedID- 24404404 | Although thalassemia, a form of chronic hemolytic anemia, is commonly associated with extramedullary hematopoiesis (emh), it is only rarely encountered in the spinal epidural space. |
| PubMedID- 23402775 | thalassemia major presents with chronic hemolytic anemia that requires regular red blood cell transfusions within the first year of life. |
| PubMedID- 25883429 | Severe hemolytic anemia in beta-thalassemia major and beta-thalassemias/hbe (beta-tm) patients requires giving blood transfusions. |
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