Browsing by Author "Villarroel S, C."

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    Guía clínica: consenso para Chile en enfermedad de Fabry
    (2012) Varas M, C.; Gómez, G.; Morales T, M.; Molt C, F.; Cabello A, J. F.; Alcántara P, A.; Downey Concha, Patricio; Barría M, C.; Álvarez C, M.; Villarroel S, C.; Ponce M, J. C.; Cortés M, F.; Moraga U, S.; Peredo O, P.
    Fabry's disease is an X-linked recessive inborn error of metabolism of glycosphingolipids, caused by the deficiency of the lisosomal enzyme alpha-galactosidase. It is a rare disease with an estimated incidence rate of approximately 1:80.000 to 1:117,000 births in the general population. Recently, the growing knowledge about this disease has permitted the development of enzyme replacement therapy, which has modified the prognosis and quality of life of these patients. In Chile, the real incidence is unknown, but the increase in the number of patients diagnosed during the last five years, mainly in the north of the country. This guide was prepared with the intention of establishing a consensus for the diagnosis, treatment and monitoring of the patients with Fabry disease based on the present available scientific evidence.