Programa de Cribado Neonatal de Enfermedades Congénitas en la Comunitat Valenciana

http://www.sp.san.gva.es/biblioteca/publicacion_dgsp.jsp?cod_pub_ran=855141620

Programa que tiene como objetivo detectar precozmente a los recién nacidos con hipotiroidismo congénito, fenilcetonuria, anemia de células falciformes o fibrosis quística para poder iniciar precozmente su tratamiento y mejorar su pronóstico.

Author(s): Aguado Codina, Cristina... [et al.] Originator(s): Generalitat Valenciana. Conselleria de Sanitat
Resource added in: 29/11/2013
Available languages: Spanish
Congenital Hypothyroidism, Cystic Fibrosis, Infant, Newborn, Metabolic Diseases, Phenylketonurias, Anemia, Sickle Cell, Genetic Diseases, Inborn
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