Scientists seek families to unlock secrets of rare eye disorders
NCT ID NCT06293560
First seen May 02, 2026 · Last updated May 16, 2026 · Updated 5 times
Summary
This study aims to learn how genetic changes contribute to microphthalmia, anophthalmia, and coloboma (MAC) in children. Researchers will collect medical histories, conduct physical exams, and analyze DNA from saliva or blood samples. Up to 3,000 children and their family members will participate to better understand these rare eye conditions.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for ANOPHTHALMIA are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Baylor College of Medicine
RECRUITINGHouston, Texas, 77030, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Conditions
Explore the condition pages connected to this study.