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Lancet ; 362(9377): 41-2, 2003 Jul 05.
Artículo en Inglés | MEDLINE | ID: mdl-12853199

RESUMEN

Stem-cell transplantation can cure beta thalassaemia. We aimed to assess whether fetal HLA typing done early in the pregnancy of couples who were at risk of beta thalassaemia could provide an alternative to pregnancy termination if the prospect of a bone-marrow transplantation from a family member was available. In our clinic in Sardinia, we did fetal HLA typing for 49 couples at risk of having a baby with beta thalassaemia. Two affected children were born and successfully received a transplantation from a family donor. Five non-affected fetuses were HLA compatible with an affected sibling and their cord blood was harvested for a future transplantation.


Asunto(s)
Enfermedades Fetales/inmunología , Trasplante de Células Madre Hematopoyéticas , Prueba de Histocompatibilidad , Talasemia beta/inmunología , Talasemia beta/terapia , Enfermedades Fetales/diagnóstico , Enfermedades Fetales/terapia , Asesoramiento Genético , Prueba de Histocompatibilidad/ética , Humanos , Diagnóstico Prenatal/ética , Factores de Riesgo , Hermanos , Talasemia beta/diagnóstico
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