Guía para el diagnóstico, seguimiento y tratamiento de la enfermedad de Fabry. / [Guidelines for diagnosis, monitoring and treatment of Fabry disease].
Medicina (B Aires)
; 73(5): 482-94, 2013.
Artigo
em Espanhol
| BINACIS
| ID: bin-132897
ABSTRACT
Fabry disease is an X-linked hereditary lysosomal storage disorder caused by deficiency of the enzyme alpha-galactosidase A. Knowledge about this disease, and its medical management, has made remarkable progress in the last decade, including the development of its specific treatment. This guide was developed by medical professionals from various specialties involved in the care of patients with Fabry disease. The discussion and analysis of the available scientific evidence, coupled with the experience of each of the participants, has allowed us to develop the concepts included in this guide in order to provide a useful tool for all professionals who care for patients with Fabry disease.
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Coleções:
Bases de dados nacionais
/
Argentina
Base de dados:
BINACIS
Assunto principal:
Doença de Fabry
Tipo de estudo:
Estudo diagnóstico
/
Guia de prática clínica
/
Pesquisa qualitativa
Idioma:
Espanhol
Revista:
Medicina (B Aires)
Ano de publicação:
2013
Tipo de documento:
Artigo