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Summary
CONGENITAL DISORDER OF GLYCOSYLATION (TSTA3)
TSTA3-CDG
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OMIM = Online Medalian Inheritance of Men

Detail information to gene locus by the National Center for Biotechnology Information NCBI:
new glycosylation disorder and treatable with
L-fucose [Huelle A 2020]
symptoms
dysmorphism
failure to thrive
feeding difficulties, poor feeding
hypotonia
onset, infancy
onset, neonatal
laboratory finding
Literature
Abbasi F,et al.A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Patients with Neonatal DiabetesCan J Diabetes002017