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Clinical Trial Summary

The investigators are inviting families to take part in a research study that will help us better understand the physical characteristics associated with children who have Microphthalmia, Anophthalmia, and Coloboma (MAC) and how changes in their DNA sequence, called genetic mutations, play a role in the risk of developing MAC


Clinical Trial Description

This study is focused on gathering data on individuals diagnosed with some of the more common visually threatening congenital eye defects collectively referred to as MAC complex; anophthalmia (total absence of the globe), microphthalmia (anomalously small eye in the orbit), and coloboma (failure of the closure of the fetal fissure). Our long-term goal is to improve prevention efforts for and clinical management of MAC. The objectives of the current study are to 1) better define the MAC phenotype and 2) characterize the role of known and newly identified pathogenic genetic variants that confer MAC susceptibility. To do this, the investigators are leveraging resources to identify MAC cases through the Texas Birth Defects Registry (TBDR), Texas Children's Hospital (TCH), and through direct referrals from our study partners. The investigators intend to conduct secondary analyses by leveraging the existing collaborative relationship with the New York State Newborn Screening Program (NYSNSP). Also, the investigators are utilizing the resources of the National Institutes of Health (NIH) Clinical Center to comprehensively phenotype cases with MAC, and the National Eye Institute (NEI) Ophthalmic Genomics Laboratory to identify genetic variants underlying MAC phenotypes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06293560
Study type Observational
Source Baylor College of Medicine
Contact
Status Recruiting
Phase
Start date September 25, 2022
Completion date September 2027

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT04833361 - Potential Environmental Causes of Uveal Coloboma
Terminated NCT00368004 - Family Studies of Uveal Coloboma
Recruiting NCT01778543 - Pathogenesis and Genetics of Microphthalmia, Anophthalmia and Uveal Coloboma (MAC)