Progress in Fabry disease / 国际儿科学杂志
International Journal of Pediatrics
;
(6): 283-286, 2010.
Artigo
em Chinês
| WPRIM
| ID: wpr-389811
ABSTRACT
Fabry disease is an inherited metabolic disease, resulting from a deficiency of the enzyme a-galactosidase A activity. Principal clinical manifestation of Fabry disease was limb pain episodes, angioceratoma, and progressive damage of heart,brain, kidney. Although Fabry disease cannot be cured at present,early diagnosis and enzyme replacement therapy can change the prognosis completely.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo de rastreamento
Idioma:
Chinês
Revista:
International Journal of Pediatrics
Ano de publicação:
2010
Tipo de documento:
Artigo
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