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Mannose supplementation in PMM2-CDG

descriptionPublicationkeyboard_double_arrow_right Article , Other literature type 11 Aug 2021Publisher:Springer Science and Business Media LLCJournal:Orphanet Journal of Rare Diseases, volume 16 (eissn: 1750-1172,

Authors: Roman Taday; Julien H. Park; Marianne Grüneberg; Ingrid DuChesne; Janine Reunert; Thorsten Marquardt;

doi: 10.1186/s13023-021-01988-x

pmid: 34380532

pmc: PMC8359111

Mannose supplementation in PMM2-CDG

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Abstract

AbstractIn this response to the letter by Witters et al., we refer to the authors' arguments regarding spontaneous enhancement of glycosylation and the claim, that mannose has no place in the treatment of PMM2-CDG. Our paper “Dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG)” has shown that further investigation of mannose in PMM2-CDG is worthwhile alongside other treatment options and should not be dismissed off-hand without the willingness to prove or disprove it in controlled prospective clinical trials.

Related Organizations

Boston Children's Hospital
United States
University Hospital Münster
Germany

Keywords

R, Congenital disorder of glycosylation, Galactose, Congenital Disorders of Glycosylation, Phosphotransferases (Phosphomutases), Dietary Supplements, Medicine, Humans, Therapy, Prospective Studies, PMM2, Letter to the Editor, Mannose

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Dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG)
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