Galactose epimerase deficiency: lessons from the GalNet registry

Galactose epimerase deficiency: lessons from the GalNet registry

Abstract Background Galactose epimerase (GALE) deficiency is a rare hereditary disorder of galactose metabolism with only a few cases described in the literature. This study aims to present the data of patients with GALE deficiency from different countries included through the Galactosemia Network t...

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Bibliographic Details
Main Authors: Britt Derks, Didem Demirbas, Rodrigo R. Arantes, Samantha Banford, Alberto B. Burlina, Analía Cabrera, Ana Chiesa, M. Luz Couce, Carlo Dionisi-Vici, Matthias Gautschi, Stephanie Grünewald, Eva Morava, Dorothea Möslinger, Sabine Scholl-Bürgi, Anastasia Skouma, Karolina M. Stepien, David J. Timson, Gerard T. Berry, M. Estela Rubio-Gozalbo
Format: Article
Language:English
Published: BMC 2022-09-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Galactose epimerase deficiency
Galactosemia type III
Galactosemias Network
Galactose-restricted diet
Online Access:https://doi.org/10.1186/s13023-022-02494-4

Internet

https://doi.org/10.1186/s13023-022-02494-4

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