Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: A case report

Kristen Westenfield, Kyriakie M Sarafoglou, Laura C Speltz, Rene Pierpont, Joan Steyermark, David R Nascene, Matthew Bower, Mary Ella M Pierpont

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Background: Congenital disorders of glycosylation are rare conditions caused by genetic defects in glycan synthesis, processing or transport. Most congenital disorders of glycosylation involve defects in the formation or transfer of the lipid-linked oligosaccharide precursor of N-linked glycans. SLC35A2-CDG (previously CDG-IIm) is caused by hemizygous or heterozygous mutations in the X-linked gene SLC35A2 that encodes a UDP-galactose transporter. To date there have only been 10 reported patients with SLC35A2 mutations. Importantly, the patient presented here was not identified in infancy by transferrin isoform analysis, the most common testing to identify patients with a congenital disorder of glycosylation. Case presentation: A 27 month old girl with developmental delay, central hypotonia, cerebral atrophy, and failure to thrive with growth retardation was identified by whole exome sequencing to have a mosaic missense variant in SLC35A2 (c.991G > A). This particular variant has been previously reported in a male as a mutation. Comparison of all clinical findings and new information on growth pattern, growth hormone testing and neurodevelopmental evaluation are detailed on the patient presented. Conclusion: This patient report increases the clinical and scientific knowledge of SLC35A2-CDG, a rare condition. New information on reduced growth, growth hormone sufficiency, lack of seizures, and neurodevelopmental status are presented. This new information will be helpful to clinicians caring for individuals with SLC35A2-CDG. This report also alerts clinicians that transferrin isoform measurements do not identify all patients with congenital disorders of glycosylation.

Original languageEnglish (US)
Article number100
JournalBMC medical genetics
Volume19
Issue number1
DOIs
StatePublished - Jun 15 2018

Bibliographical note

Publisher Copyright:
© 2018 The Author(s).

Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.

Keywords

  • Congenital disorder of glycosylation
  • Growth failure
  • SLC35A2 mutation
  • Transferrin isoforms
  • Whole exome sequencing
  • Inborn errors of metabolism

PubMed: MeSH publication types

  • Case Reports
  • Journal Article

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