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

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) showe...

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Detalhes bibliográficos
Publicado no:JIMD Rep
Main Authors: Abdel Ghaffar, Tawhida Y., Ng, Bobby G., Elsayed, Solaf M., El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2020
Assuntos:
Case Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7653262/
https://ncbi.nlm.nih.gov/pubmed/33204592
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12159
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