About WhatIsLCA
This website was created to help LCA patients and their families better understand the disease, access the latest research, and find support resources.
Our Mission
Leber Congenital Amaurosis is a rare inherited retinal disease that affects families worldwide. Information about LCA is often scattered across medical journals, clinical databases, and specialist websites — making it difficult for patients and families to get a clear, comprehensive picture.
WhatIsLCA aims to bridge this gap by providing evidence-based, accessible information about LCA in one place — from understanding the genetics to following the latest gene therapy breakthroughs.
Evidence-Based Content
All medical information on this website is sourced from peer-reviewed publications and authoritative medical databases. Key sources include:
Medical Disclaimer
This website is for educational and informational purposes only. It does not provide medical advice, diagnosis, or treatment.
The information provided here should not be used as a substitute for professional medical advice. Always seek the guidance of a qualified healthcare provider with any questions you may have regarding LCA or any other medical condition.
Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
Treatment information, including clinical trial status, is provided for awareness purposes and may not reflect the most current state. Always verify treatment availability and eligibility with your medical team.
Privacy & Open Source
This website does not collect personal data, use tracking cookies, or serve advertisements. It is built as a community resource for LCA families worldwide.