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...

Descripción completa

Detalles Bibliográficos
Autores principales: Abdel Ghaffar, Tawhida Y., Ng, Bobby G., Elsayed, Solaf M., El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653262/
https://www.ncbi.nlm.nih.gov/pubmed/33204592
http://dx.doi.org/10.1002/jmd2.12159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653262/
https://www.ncbi.nlm.nih.gov/pubmed/33204592
http://dx.doi.org/10.1002/jmd2.12159

Ejemplares similares