α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females

Volume: 501, Pages: 27 - 32
Published: Feb 1, 2020
Abstract
Fabry disease (FD [MIM:301500]) is an X-linked lysosomal storage disorder caused by mutations in the GLA gene. Deficient activity of its product, lysosomal enzyme α-galactosidase A (α-Gal A), leads to excessive accumulation of glycosphingolipids in cells of multiple organs. The establishing of the diagnosis is challenge in female patients because of milder clinical manifestation and normal α-Gal A activity. The globotriaosylsphingosine (lysoGb3)...
Paper Details
Title
α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females
Published Date
Feb 1, 2020
Volume
501
Pages
27 - 32
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