Genetic and Functional Analysis of Aplasia Cutis Congenital (ACC)

NCT01630421 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2026-04-15

No results posted yet for this study

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.

Conditions

  • Aplasia Cutis Congenita

Sponsors & Collaborators

  • UConn Health

    lead OTHER

Principal Investigators

  • Ernst J Reichenberger, PhD · UConn Health

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2030-12-31
Completion
2030-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01630421 on ClinicalTrials.gov