| Literature DB >> 9107524 |
C Pászty1.
Abstract
Sickle cell anemia and the thalassemias are globally the most common class of inherited disorders. Current treatment options are limited (transfusion, iron chelation) and are not suited to large-scale use in developing countries where the population of affected individuals is expected to undergo a tremendous increase in the near future. As such, the development of more practical and more permanent therapies is urgently needed. Recently, transgenic and gene knock-out technologies have been used to create mouse models for sickle cell anemia and all of the clinically relevant thalassemias (hemoglobin Bart's hydrops fetalis, hemoglobin H disease, beta-thalassemia intermedia, beta-thalassemia major/Cooley's anemia). These newly developed murine models should play an important role in the development of improved approaches for treating these commonly occurring genetic diseases.Entities:
Mesh:
Year: 1997 PMID: 9107524 DOI: 10.1097/00062752-199704020-00003
Source DB: PubMed Journal: Curr Opin Hematol ISSN: 1065-6251 Impact factor: 3.284