# Congenital diarrhea and enteropathies caused by a heterozygous mutation in the GUCY2C gene: a rare case report

## TL;DR

A rare case of congenital diarrhea in an infant was linked to a mutation in the GUCY2C gene, with successful management through specialized care.

## Contribution

Identification of a novel heterozygous GUCY2C mutation as a cause of congenital diarrhea in a Chinese infant.

## Key findings

- A heterozygous mutation in GUCY2C (c.2356T > C, p.Y786H) was found to cause congenital diarrhea and enteropathies.
- The patient showed normal growth and symptom resolution with supportive care and formula adjustments.
- Genetic testing was crucial in diagnosing the rare condition and guiding treatment.

## Abstract

This report presents a rare case of congenital diarrhea and enteropathies in a Chinese infant caused by a heterozygous mutation in the GUCY2C gene.

A male infant was born prematurely with a history of polyhydramnios and prenatal intestinal dilation. He developed persistent abdominal distension, secretory diarrhea, metabolic acidosis, severe electrolyte imbalances, and failure to thrive. Whole-exome sequencing identified a heterozygous mutation in GUCY2C (c.2356T > C, p.Y786H), classified as likely pathogenic. The patient also exhibited intestinal malrotation but did not require surgical intervention. Management included total parenteral nutrition, transition to an amino acid-based formula, and extensive electrolyte supplementation. At the 72-month follow-up, he exhibited normal growth and complete resolution of gastrointestinal symptoms.

A heterozygous mutation in the GUCY2C gene (c.2356T > C) was identified as the cause of this rare congenital diarrheal disorder. These findings emphasize the essential function of genetic testing in children with chronic, treatment-refractory diarrhea and highlight the potential for excellent long-term outcomes with suitable supportive care.