Scientists dig into DNA of rare childhood gut disease
NCT ID NCT01114035
First seen Mar 10, 2026 · Last updated Jun 16, 2026 · Updated 14 times
Summary
This study aimed to better understand a rare bowel disease called intestinal epithelial dysplasia (tufting enteropathy) by looking at the genes and physical traits of affected children. Researchers studied 41 children, ages 0 to 15, who were being evaluated for an intestinal transplant. The goal was to identify the genes and mutations responsible for the condition, not to test a new treatment.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Necker Hospital
Paris, 75015, France
Conditions
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