Anemia falciforme: una revisión sobre el genotipo de la enfermedad, haplotipos, diagnóstico y estudios asociados
- Autores: Marcela Diaz Matallana, Yusselfy Márquez Benítez, Julio César Martínez Lozano, Ignacio Briceño Balcázar, Escilda Benavides-Benítez, Jaime E. Bernal
- Localización: Revista Médica de Chile, ISSN-e 0034-9887, Vol. 149, Nº. 9, 2021, págs. 1322-1329
- Idioma: español
- Títulos paralelos:
- Disease genotype, haplotypes, diagnosis and associated studies in sickle cell anemia
- Enlaces
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Resumen
Sickle cell anemia is a type of hemoglobinopathy characterized by a specific mutation in the beta globin gene with the consequent generation of an unstable hemoglobin that crystallizes in a state of hypoxia. This causes a change in the structure of the red blood cell, which ends up producing vaso-occlusion with the corresponding clinical complications for the patient. Worldwide, various diagnostic tests have been developed that allow the appropriate approach to the affected patient. These include techniques for the determination of hemoglobin and the use of molecular markers, among others. There are new therapeutic alternatives to the use of hydroxyurea and L-glutamine, such as the use of gene therapy tools. The most recent experimental trials are exploring gene editing techniques.
