Resources
Resources for PCDH19 Researchers
The PCDH19 Alliance is committed to supporting and collaborating with researchers who are working to deepen our understanding of PCDH19-related epilepsy. Whether you’re studying the gene, exploring treatment strategies, or working on clinical care improvements, your work plays a vital role in shaping the future for those living with this rare condition.
Research Support
Advancing research is essential to uncovering the mechanisms behind the condition, identifying potential treatments, improving outcomes for individuals and families, and finding a cure.
PCDH19 Research Funding
We provide grants for promising research projects focused on understanding and treating PCDH19. If you’re a researcher with a proposal that aligns with our mission, we invite you to apply for funding.
Alliance-Funded Research
We are proud to fund innovative, high-impact research that aims to improve understanding, diagnosis, and treatment of PCDH19-related epilepsy.
Patient & Family Registry
Connect with our patient community through our registry to support recruitment, data collection, and longitudinal studies.
PCDH19 Professional and Family Conference
Present your work at the biennial PCDH19 Professional and Family Conference and connect directly with families, clinicians, and other researchers.
Resources
View our science and research resources.
New Treatments – How Much Longer?
After months – maybe even years – of feeling like a hamster on its exercise wheel chasing a solution to...
PCDH19 Genetics 3: X-Chromosome Inactivation & Mosaicism
Learn more about the X-chromosome inactivation and Mosaicism related to PCDH19. This is the third in an ongoing series of...
PCDH19 Genetics 2: Inheritance
Learn more about the inheritance of genes related to PCDH19. This is the second in an ongoing series of instructional...
Join the Alliance
Join the PCDH19 Alliance to stay informed of funding opportunities and make connections with PCDH19 families. Your work is critical to advancing understanding and improving lives, and we’re here to support and amplify it.