Percc1-Associated Congenital Diarrhea and Enteropathy: Description of a Novel Variant

Persistent diarrhea that occurs in the first weeks of life and is caused by monogenic defects are defined as congenital diarrhea and enteropathies (CoDEs). The PERCC1 (proline and glutamate-rich protein with coiled-coil domain 1) gene which has a role in development of enteroendocrine cells, was recently found to be associated with CoDEs. We report the clinical, laboratory, and histopathologic findings of CoDE caused by a novel, homozygous variant (c.337 del) in the second exon of PERCC1 gene in an infant diagnosed at 2 months postnatally. The unique findings in our case were the location and/or distribution abnormality of enteroendocrine cells and exocrine pancreatic insufficiency. We can conclude that these distinctive features may expand the spectrum of PERCC1-associated CoDE.

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Publication Details

Journal
Pediatric and Developmental Pathology
Published
2026-05-31
DOI
https://doi.org/10.1177/10935266261450257
Primary Topic
Celiac Disease Research and Management
Type
article
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article

Percc1-Associated Congenital Diarrhea and Enteropathy: Description of a Novel Variant

Ahsen Dönmez Türkmen, Deniz Ertem, Esra Dirimtekin, Çiğdem Çelikel et al.
Pediatric and Developmental Pathology
Celiac Disease Research and Management
article

Percc1-Associated Congenital Diarrhea and Enteropathy: Description of a Novel Variant

Ahsen Dönmez Türkmen, Deniz Ertem, Esra Dirimtekin, Çiğdem Çelikel, İbrahim Bagci, Emine Celik, Bilge S. Akkelle
article en

Abstract

Persistent diarrhea that occurs in the first weeks of life and is caused by monogenic defects are defined as congenital diarrhea and enteropathies (CoDEs). The PERCC1 (proline and glutamate-rich protein with coiled-coil domain 1) gene which has a role in development of enteroendocrine cells, was recently found to be associated with CoDEs. We report the clinical, laboratory, and histopathologic findings of CoDE caused by a novel, homozygous variant (c.337 del) in the second exon of PERCC1 gene in an infant diagnosed at 2 months postnatally. The unique findings in our case were the location and/or distribution abnormality of enteroendocrine cells and exocrine pancreatic insufficiency. We can conclude that these distinctive features may expand the spectrum of PERCC1-associated CoDE.

Pediatric and Developmental Pathology
Marmara University (TR)
Good health and well-being
Openalex Percentile: Top 5%
Celiac Disease Research and Management
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Percc1-Associated Congenital Diarrhea and Enteropathy: Description of a Novel Variant — Ahsen Dönmez Türkmen, Deniz Ertem, et al. · Pediatric and Developmental Pathology (2026) | TGRS Research Map | TGRS