PedAM
Pediatric Disease Annotations & Medicines
| Disease | thalassemia |
| Phenotype | C0002895|sickle cell anemia |
| Sentences | 5 |
| PubMedID- 22065975 | The interaction of α-thalassemia with sickle cell anemia (hemoglobin ss disease, hbss) is known to influence hematological indices, reduce hemolytic rate and intravascular sickling, and increase deformation of the red blood cells. |
| PubMedID- 25869286 | The thalassemias, together with sickle cell anemia and its variants, are the world's most common form of inherited anemia, and in economically undeveloped countries, they still account for tens of thousands of premature deaths every year. |
| PubMedID- 20712767 | The thalassemias, together with sickle cell anemia and its variants, are by far the most common monogenic diseases. |
| PubMedID- 24324305 | However, when group i (beta thalassemia) was compared with group ii (sickle cell anemia), results were found to highly significant (p<0.001) only for decayed missing filled tooth. |
| PubMedID- 24399969 | Found significantly increased plasma concentrations of anti-spectrin nabs in splenectomized patients with β-thalassemia major and in patients with sickle cell anemia (wiener et al., 1986). |
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