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Article

A New Case of Congenital Malabsorptive Diarrhea and Diabetes Secondary to Mutant Neurogenin-3.

Pediatrics - 1 Aug 2017

Germán-Díaz Marta, Rodriguez-Gil Yolanda, Cruz-Rojo Jaime, Charbit-Henrion Fabienne, Cerf-Bensussan Nadine, Manzanares-López Manzanares Javier, Moreno-Villares José Manuel

Abstract excerpt

Congenital diarrheal disorders are a group of rare enteropathies that often present with life-threatening diarrhea in the first weeks of life. Enteric anendocrinosis, characterized by a lack of intestinal enteroendocrine cells due to recessively inherited mutations in the Neurogenin-3 (NEUROG3) gene, has been described as a cause of congenital malabsorptive diarrhea. Diabetes mellitus also is typically associated...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28724572
DOI: 10.1542/peds.2016-2210

Genes

NEUROG3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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