Scientists hunt for genes behind rare skin condition
NCT ID NCT01630421
First seen Apr 28, 2026 · Last updated May 25, 2026 · Updated 4 times
Summary
This research study aims to find the genes and genetic changes that cause aplasia cutis congenita (ACC), a rare condition where skin is missing at birth. Researchers will study DNA and tissue samples from up to 600 people with ACC and their family members. The goal is to better understand what causes the disorder and how it progresses.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University of Connecticut Health Center
RECRUITINGFarmington, Connecticut, 06030, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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