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MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature

Title: MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature
Authors: Abdel Ghaffar, Tawhida Y.; Ng, Bobby G.; Elsayed, Solaf M.; El Naghi, Suzan; Helmy, Sarah; Mohammed, Nermine; El Hennawy, Ahmed; Freeze, Hudson H.
Contributors: National Institutes of Health
Source: JIMD Reports ; volume 56, issue 1, page 20-26 ; ISSN 2192-8312 2192-8312
Publisher Information: Wiley
Publication Year: 2020
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: MPI‐CDG is a rare congenital disorder of glycosylation (CDG) which presents with hepato‐gastrointestinal symptoms and hypoglycemia. We report on hepatic evaluation of two pediatric patients who presented to us with gastrointestinal symptoms. Analysis of carbohydrate deficient transferrin (CDT) showed a Type 1 pattern and molecular analysis confirmed the diagnosis of MPI‐CDG. Oral mannose therapy was markedly effective in one patient but was only partially effective in the other who showed progressive portal hypertension.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1002/jmd2.12159
Availability: https://doi.org/10.1002/jmd2.12159; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjmd2.12159; https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12159; https://onlinelibrary.wiley.com/doi/full-xml/10.1002/jmd2.12159
Rights: http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.6C5F37BC
Database: BASE