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Trials / Completed

CompletedNCT03892798

Database Of Clinical Data For Individuals With Variants In The IRF2BPL Gene

Status
Completed
Phase
Study type
Observational
Enrollment
34 (actual)
Sponsor
Children's Hospital Medical Center, Cincinnati · Academic / Other
Sex
All
Age
2 Months – 80 Years
Healthy volunteers
Not accepted

Summary

This protocol serves as a data collection tool for individuals with variants (missense, nonsense, frameshifts) in the IRF2BPL gene (MIM 611720), which causes Neurodevelopmental Regression, Seizures, Autism and Developmental Delay (NEDAMSS, MIM 618088) and may be involved in other neurodevelopmental presentations. This information will be analyzed to develop a better understanding of the findings and progression of symptoms in individuals with variants in the IRF2BPL gene.

Detailed description

Neurodevelopmental Regression, Abnormal Movements, Loss of Speech, and Seizures (NEDAMSS) is caused by changes in the IRF2BPL gene. Variants in the gene can also lead to other neurodevelopmental presentations. Due to the limited number of cases that have been described to date, clinicians may have a limited understanding of what types of symptoms can develop in affected individuals and at what age. The purpose of the study is to gather clinical information about progression, treatments and outcomes for patients with variants in IRF2BPL. The investigators will collect information about medical history, growth, development, treatments and the results of previous genetic tests. In some cases, the investigators may also collect tissue samples. This is a non-interventional study that will expand the current understanding of the range of health concerns that can be seen in individuals with changes in the IRF2BPL gene by collecting medical information and samples from a larger group of affected individuals.

Conditions

Interventions

TypeNameDescription
OTHERNo interventions are plannedNo interventions are planned

Timeline

Start date
2018-11-27
Primary completion
2024-05-17
Completion
2024-05-17
First posted
2019-03-27
Last updated
2024-05-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03892798. Inclusion in this directory is not an endorsement.

Database Of Clinical Data For Individuals With Variants In The IRF2BPL Gene (NCT03892798) · Clinical Trials Directory