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Article

Congenital disorder of glycosylation Ib (CDG-Ib) without gastrointestinal symptoms.

Journal of inherited metabolic disease - 1 Jan 2003

Penel-Capelle D, Dobbelaere D, Jaeken J, Klein A, Cartigny M, Weill J

Abstract excerpt

We report a 7-year-old girl with hyperinsulinaemic hypoglycaemia and hepatomegaly due to congenital disorder of glycosylation (CDG) Ib without gastrointestinal symptoms. Oral mannose therapy produced clinical and biochemical normalization after 2 years of treatment.

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Identifiers

PMID: 12872847
DOI: 10.1023/a:1024044017385

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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