A resource for families affected by ITSN1 genetic variations
If you or your child has been diagnosed with an ITSN1 gene mutation, you're not alone. This website provides information, research links, and a growing community of support for families navigating this genetic condition.
Our goal is to help families understand what ITSN1 is, connect with ongoing research, and eventually build a supportive community.
Learn about the groundbreaking research being conducted by the Dhindsa Lab at Baylor College of Medicine on ITSN1 gene mutations and their impact on neurological development.
This important study is advancing our understanding of ITSN1 and bringing hope for personalized treatments.
Families affected by ITSN1 mutations are partnering with researchers to advance understanding and treatment. Read about how one family's journey with Dr. Dhindsa's lab at Texas Children's Hospital is helping to unlock new possibilities for personalized care.
Read Owen's Story