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Rare syndrome study aims to map dental and facial patterns

NCT ID NCT07476417

First seen Mar 22, 2026 · Last updated Apr 30, 2026 · Updated 7 times

Summary

This study looks at the teeth, mouth, and face of people with Mowat-Wilson syndrome, a rare genetic condition. Researchers will check for cavities, gum disease, and facial differences, and ask about quality of life. No treatments are tested—only observations are made. About 25 people with a confirmed ZEB2 gene change will take part.

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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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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • University of Milan

    Milan, Italy

    Contact Email: •••••@•••••

    Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.