NCT02447861

The 3q29 Deletion and 3q29 Duplication: Architecture of Behavioral Phenotypes

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 800 (estimated)
• Sponsor: Rutgers, The State University of New Jersey · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Accepted

Summary

The 3q29 deletion syndrome is caused by a deletion of a small part of human chromosome 3, and the duplication syndrome is caused by a duplication of this same small region. The purpose of this study is to understand the medical and behavioral consequences of these syndromes.

Detailed description

People with 3q29 deletion syndrome are missing a small part of a region on human chromosome 3, and people with 3q29 duplication syndrome have an extra part of their chromosome 3. Sometimes babies are born with a deletion or duplication of part of human chromosome 3, even though their parents have an intact chromosome 3. This is called de novo (or new) abnormalities.

Conditions

• Microdeletion 3q29 Syndrome
• Microduplication 3q29 Syndrome

Timeline

• Start date: 2013-07-01
• Primary completion: 2028-01-01
• Completion: 2028-01-01
• First posted: 2015-05-19
• Last updated: 2024-12-06

Locations

1 site across 1 country: United States