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.
Article
in Spanish
| 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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Collection:
National databases
/
Argentina
Database:
BINACIS
Main subject:
Fabry Disease
Type of study:
Diagnostic study
/
Practice guideline
/
Qualitative research
Language:
Spanish
Journal:
Medicina (B Aires)
Year:
2013
Document type:
Article