Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The purpose of this study is to establish a registry of individuals with confirmed or suspected Chopra-Amiel-Gordon Syndrome (CAGS) to learn more about the range of symptoms, changes in the structure of the brain seen on imaging, and learning difficulties that individuals with this disorder may experience. The investigators will obtain medical history, family history, MRI records, patient photographs, and genetic test results from individuals with confirmed or suspected CAGS. A subset of participants will also undergo a standardized neurobehavioral assessment. This data will be maintained on a secure research database. Sample collection will be offered to participants for the functional testing and the generation of iPSC cell lines, for neuronal reprogramming and phenotyping.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Participants must have a known or suspected diagnosis of CAGS

• Participants with a known diagnosis or CAGS have a disease-causing (likely pathogenic or pathogenic) variant in ANKRD17 evidenced by a pre-existing clinical genetic report.

• Participants with a suspected diagnosis of CAGS must have a variant of uncertain significance in CAGS evidenced by a pre-existing clinical genetic report and clinical features of CAGS

Locations
United States
Massachusetts
Boston Children's Hospital
RECRUITING
Boston
Contact Information
Primary
Maya Chopra, MBBS FRACP
maya.chopra@childrens.harvard.edu
617-919-6258
Backup
Raymond Belanger Deloge, MS, CGC
Raymond.belangerdeloge@childrens.harvard.edu
Time Frame
Start Date: 2022-08-27
Estimated Completion Date: 2026-12-01
Participants
Target number of participants: 60
Treatments
Proband
Study participants who have suspected or confirmed CAGS based on having a variant of uncertain significance, likely pathogenic variant, or pathogenic variant in ANKRD17 and clinical features of the condition.
Unaffected family members
Family members of the proband who do not have an ANKRD17 variant.
Sponsors
Leads: Boston Children's Hospital

This content was sourced from clinicaltrials.gov

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