White matter lesions in fabry disease before and after enzyme replacement therapy: a 2-year follow-up

FLAVIO FRANCIOSI AESSE, laura B. Jardim, Leonardo M. Vedolin, Maria G. Burin, Claudia Cecchin, Cristina B. O. Netto, Ursula S. Matte, Fernanda Pereira, Luciane kalakin, Roberto Giugliani, JOÃO MARCONATO, CLAUDIO DE FARIA PITTA PINHEIRO

Arquivos de Neuropsiquiatria, v. 64, n. 3-b, p. 711-717, 2006.

Motivo: Produção Corpo Clínico

Setor HMV: UDI - Gerência

Área da saúde: Radiologia e Diagnóstico por Imagem

Resumo: Purpose: To report the clinical and neuroimaging, central nervous system (CNS) findings of patients with Fabry disease (FD) during 24 months of enzyme replacement therapy (ERT) with agalsidasealpha. Method: Eight patients were included. Six completed 24 months of ERT. Clinical and magnetic resonance imaging (MRI) data were obtained at 0, 12 and 24 months of ERT. White matter lesions (WML) were evaluated as well as their relation to age, symptoms and neurological examination (CNS score). Results: MRI was stable in 3 patients. WML and CNS score worsened in one patient, fluctuated in another, and improved in the sixth patient. In the whole series, there were 15 WML at baseline, and 19 at the 24th month. In two years, 4 lesions disappeared, whereas 8 appeared. Conclusion: A widespread pattern of silent WML in FD was seen. In two years, some WML appeared, and some disappeared. If these phenomena were related to the natural history, remains to be demonstrated.

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