## ABSTRACT Fabry disease is a multisystem disorder associated with wide variability in clinical expression. Fabry disease is an X‐linked lysosomal storage disorder caused by a deficiency of α‐galactosidase A. The enzyme defect leads to the systemic accumulation of glycosphingolipids with α‐galacto
✦ LIBER ✦
Enzyme replacement therapy for Morquio
✍ Scribed by Alexander Rodríguez; Ángela J. Espejo; Alejandra Hernández; Olga L. Velásquez; Lina M. Lizaraso; Henry A. Cordoba; Oscar F. Sánchez; Carlos J. Alméciga-Díaz; Luis A. Barrera
- Publisher
- Springer-Verlag
- Year
- 2010
- Tongue
- English
- Weight
- 486 KB
- Volume
- 37
- Category
- Article
- ISSN
- 1476-5535
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## Abstract We prospectively evaluated the effect of enzyme replacement therapy (ERT) on the intraepidermal nerve fiber density (IENFD) and thermal threshold in patients with Fabry disease, an X‐linked disorder associated with a painful small‐fiber neuropathy and decreased linear IENFD in a length‐