Amico Luisa, Visconti Giuseppe, Amato Antonio, Azzolina Vitalba, Sessa Adalberto, Li Vecchi Maurizio
Operative Unit of Nephrology and Dialysis, V. Cervello Hospital, Palermo - Italy.
J Nephrol. 2005 Nov-Dec;18(6):770-2.
Anderson-Fabry disease is a rare inborn X-linked glycosphingolipid storage disorder in which the deficient activity of the enzyme alfa-galactosidase A (alfa-gal A) leads to the progressive tissular accumulation of lipidic molecules which, in turn, cause a protean pattern of multi-organ disfunction. Enzyme replacement therapy has recently become available and has proved to be effective in controlling the disorder. We present and discuss the case of a family with this disease, with special attention to the variability of clinical features and the difficulty of a correct diagnosis.
安德森-法布里病是一种罕见的先天性X连锁鞘糖脂贮积病,其中α-半乳糖苷酶A(α-gal A)活性不足导致脂质分子在组织中进行性蓄积,进而引起多器官功能障碍的多种表现形式。酶替代疗法最近已可应用,并已证明在控制该疾病方面有效。我们展示并讨论了一个患有这种疾病的家庭的病例,特别关注临床特征的变异性和正确诊断的困难。