Scientists hunt for genes behind rare skin condition
NCT ID NCT01630421
First seen Apr 28, 2026 · Last updated May 15, 2026 · Updated 2 times
Summary
This study aims to find the genes that cause aplasia cutis congenita (ACC), a rare condition where babies are born with missing patches of skin. Researchers will analyze DNA and tissue samples from 600 participants, including affected individuals and their family members. The goal is to better understand what causes ACC, 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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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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