Microvillus Inclusion Disease Variant in an Infant with Intractable Diarrhea

Microvillus inclusion disease (MVID) is a rare autosomal recessive congenital enteropathy characterized by intractable secretory diarrhea. We report a case of MVID variant with a homozygous gene mutation in syntaxin 3 (STX3). The patient is a male Saudi infant who presented shortly after birth with...

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Detalles Bibliográficos
Autores principales: Alsaleem, Badr M. Rasheed, Ahmed, Amna Basheer M., Fageeh, Musa Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2017
Materias:
Single Case
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731099/
https://www.ncbi.nlm.nih.gov/pubmed/29282386
http://dx.doi.org/10.1159/000479624

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731099/
https://www.ncbi.nlm.nih.gov/pubmed/29282386
http://dx.doi.org/10.1159/000479624

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