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Prevention, diagnosis and services.
Bermejo, Eva; Martínez-Frías, María Luisa.
Afiliación
  • Bermejo E; Rare Diseases Research Institute (IIER), Instituto de Salud Carlos III, Madrid, Spain. eva.bermejo@isciii.es
Adv Exp Med Biol ; 686: 55-75, 2010.
Article en En | MEDLINE | ID: mdl-20824439
ABSTRACT
This chapter summarizes how prevention, diagnosis and services can result from the activities of a research programme on the group of rare diseases constituted by congenital anomalies. The Spanish Collaborative Study of Congenital Malformations (ECEMC) is a research programme based on a case-control registry of consecutive newborn infants with congenital anomalies. Its aim is the prevention of this group of rare diseases, through the research on their causes and pathogenesis, combined with the translational activity to transfer the benefits of this knowledge to the general population and health care providers. Its experience could be applied to the research on other rare diseases. The different levels of prevention (primary, secondary, tertiary and quaternary) are briefly defined, and the way in which these levels are being applied or can be applied to congenital defects prevention is reviewed. The main primary prevention measures regarding congenital anomalies are also detailed. To this respect, the benefits derived from the activity of Teratology Information Services (TIS), for the general population as well as for health care providers, are explained. It is finally emphasized how the epidemiological data can contribute to the prevention of that group of rare diseases.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Congénitas / Enfermedades Raras Tipo de estudio: Diagnostic_studies / Observational_studies Límite: Female / Humans / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Adv Exp Med Biol Año: 2010 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Congénitas / Enfermedades Raras Tipo de estudio: Diagnostic_studies / Observational_studies Límite: Female / Humans / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Adv Exp Med Biol Año: 2010 Tipo del documento: Article País de afiliación: España
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