RecruitingNCT01630421
Genetic and Functional Analysis of Aplasia Cutis Congenital (ACC)
Identification of Mutations That Lead to Aplasia Cutis Congenita in Families and Isolated Cases and Studies of Cellular and Molecular Mechanisms
Sponsor
UConn Health
Enrollment
600 participants
Start Date
Apr 1, 2009
Study Type
OBSERVATIONAL
Conditions
Summary
The goal of this research study is to identify genes and regulatory elements on chromosomes that cause ACC. The investigators also study tissue samples from patients to learn about the processes that lead to this disorder.
Eligibility
Inclusion Criteria1
- ACC; unaffected individuals only if part of a participating ACC family
Exclusion Criteria1
- No ACC unaffected individuals only as part of a participating ACC family
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT01630421