Fabry disease and kidney involvement: starting from childhood to understand the future
Abstract
The accumulation of globotriaosylceramide (Gb-3) in multiple organs, such as the heart, kidney, and nervous system, due to mutations in the galactosidase alpha (GLA) gene, represents the key point of Fabry disease (FD). The common symptoms appear in childhood or adolescence, including neuropathic pain, angiokeratoma, acroparesthesia, and corneal opacities. A multi-organ involvement induces a significant deterioration in the quality of life with...
Paper Details
Title
Fabry disease and kidney involvement: starting from childhood to understand the future
Published Date
Apr 30, 2021
Journal
Volume
37
Issue
1
Pages
95 - 103
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