Characterization and Natural History of Williams Syndrome and Other Chromosome 7q11.23 Variants

NCT ID: NCT06930417

Last Updated: 2025-04-16

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 2000 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-10-21
• Study Completion Date: 2045-10-21

Brief Summary

The goal of this observational natural history study is to better characterize development, transition to adulthood, health and behavior of individuals diagnosed with Williams syndrome (WS) or carrying other variants of 7q11.23 chromosome and to build a DNA and tissue biobank with samples donated by affected individuals. The study has multiple arms focused on different aspects of WS. Participants with genetic diagnosis of WS or other variants of 7q11.23 and their family members are eligible to participate. Study participants may participate in one or multiple arms of the study:

1. Natural History Genotype-Phenotype Study to test the hypothesis that health, behavior, and developmental variability observed in WS is determined by genetic factors and to characterize those genetic changes. Participants of all ages are eligible to participate. Either a blood or saliva sample is required for participation.

2. Biobank: the research team is building a biobank enabling the development of new laboratory tools and models to study WS and test new treatment approaches. A blood sample is required for participation. Participants of all ages are eligible to participate.

3. Development arm of the study aims to delineate the development of language, cognition, personality, literacy and mathematics skills, and adaptive behavior from very early childhood through adulthood in individuals who have WS or Dup7. The purpose of this study also includes determining the predictors of specific aspects of development (e.g., word reading ability, language ability, spatial ability) for individuals with WS or Dup7. Affected individuals of all ages are eligible to participate.

4. Transition to Adulthood study aims to understand how young adults with WS make a successful transition out of high school into adulthood and to help them in this journey by providing a comprehensive psychosocial transition coupled with a medical transition plan. Individuals ages 14-25 years old are eligible to participate. Study requires three in person visits.

Conditions

Williams Beuren Syndrome; Williams Syndrome; Williams Beuren Region Duplication; Dup7

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• clinical and/or molecular diagnosis of Williams syndrome (WS)
• biological parents or siblings of individuals diagnosed with WS
• molecular diagnosis of 7q11.23 duplication syndrome (Dup7)
• molecular diagnosis of another abnormality in the 7q11.23 region

Exclusion Criteria

• No diagnosis of abnormalities in the 7q11.23 region, while not being a biological relative of affected individuals

• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Children's Hospital of Philadelphia

OTHER

Sponsor Role: collaborator

University of Pennsylvania

OTHER

Sponsor Role: lead

Responsible Party

Dasha Fleyshman

Research Program Manager

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Daniel Rader, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

Carolyn Mervis, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

Edward Brodkin, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

Benjamin Yerys, PhD

Role: PRINCIPAL_INVESTIGATOR

Children's Hospital of Philadelphia

Locations

University of Pennsylvania

Philadelphia, Pennsylvania, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Dasha Fleyshman, PhD

Role: CONTACT

dasha.fleyshman@pennmedicine.upenn.edu

267-449-8075

Armellino Center of Excellence for Williams syndrome

Role: CONTACT

aceforws@pennmedicine.upenn.edu

Facility Contacts

Dasha Fleyshman, PhD

Role: primary

dasha.fleyshman@pennmedicine.upenn.edu

267-449-8075

Armellino Center of Excellence for Williams syndrome

Role: backup

aceforws@pennmedicine.upenn.edu

Other Identifiers

23-020775

Identifier Type: OTHER

Identifier Source: secondary_id

851719

Identifier Type: -

Identifier Source: org_study_id