RESUMEN

Two new cases of hemoglobin S-beta thalassemia are being reported. Twenty-six relatives are studied. The two cases were classified as Mediterranean variety. The diagnostic problem and the therapeutical possibilities are considered.

Asunto(s)

Talasemia/genética , Femenino , Hemoglobinas Anormales/análisis , Humanos , Masculino , México , Linaje , Talasemia/sangre , Talasemia/inmunología