Understanding the genetic causes of 22q11.2 Deletion Syndrome

Molecular Dissection of the 22q11.2 Deletion Syndrome

NIH-funded research Children's Hosp of Philadelphia · NIH-11100054

This study is looking at the genes linked to 22q11.2 Deletion Syndrome to help us understand how it affects kids' health, with the hope of finding better ways to diagnose and treat those who have it.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionChildren's Hosp of Philadelphia NIH-funded
Lab location1 site (Philadelphia, United States)
Project IDNIH-11100054 on NIH RePORTER

What this research studies

This research investigates the genetic underpinnings of 22q11.2 Deletion Syndrome, a condition that can lead to various health issues in children. By using advanced optical mapping technology, the study aims to accurately characterize the complex genomic region associated with this syndrome. The goal is to better understand how these genetic changes occur and their impact on health, which could lead to improved diagnosis and treatment options for affected individuals.

Who could benefit from this research

Good fit: Ideal candidates for this research are children aged 0-11 years who have been diagnosed with 22q11.2 Deletion Syndrome.

Not a fit: Patients who do not have 22q11.2 Deletion Syndrome or are outside the age range of 0-11 years may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could provide critical insights that lead to better management and treatment strategies for children with 22q11.2 Deletion Syndrome.

How similar studies have performed: Previous research has shown success in using optical mapping technologies to investigate complex genomic regions, suggesting that this approach may yield valuable insights.

Where this research is happening

Philadelphia, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions 22q11 Chromosomal Microdeletion Syndrome22q11 Deletion Syndrome22q11.2 deletion syndrome
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.