article
Mutaciones heterocigóticas en el gen de la ?-galactosidasa A en dos pacientes con ACV criptogénico
Autor
Peña-Guzmán, Laura Lucia
Rodriguez-Quintana, Jesús Hernán
Ojeda-Moncayo, Clímaco Ernesto
Institución
Resumen
SUMMARY Fabry's disease is a recessive X linked genetic disorder in which lysosomal enzyme alpha-galactosidase A activity is affected, with accumulation of different kind of metabolites such as globotriaosylceramide and the deacylated globotriaosylceramide which are responsible for the multi-organ dysfunction that is seen in this disease, and also of the several phenotypic manifestations, mainly in nervous system, skin, gastrointestinal tract, heart and kidney. Earlier neurological manifestation is neuropathic pain could finding also gastrointestinal tract, skin and eye complaints while Cardiac and renal damage present later like as cerebrovascular disease which presents in adulthood. Two clinical cases of young patients with cryptogenic stroke with heterozygous mutations for Fabry's disease are presenting below.