As part of our ongoing efforts to advance research and treatment options for Lafora disease, we invite you to contribute to our Patient Mutation Database. Your participation is crucial in comprehensively understanding this rare genetic disorder.
Contact us with any questions!
Report Lafora Mutations
If you encounter a novel mutation, please fill out the following form! You will help provide valuable insights into the genetic landscape of Lafora disease, ultimately aiding in developing targeted therapies and improving patient outcomes. Thank you for supporting our mission to improve the lives of those affected by Lafora disease.
Access the Database
Researchers and scientists, we want this to be freely available for you. Please complete this form to access the database of reported Lafora mutations.
The mission of Chelsea’s Hope is to improve the lives of those affected by Lafora Disease and help accelerate the development of treatments.
Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 non-profit organization. EIN: 27-1008382
Chelsea’s Hope, Post Office Box 348626, Sacramento, CA 95834
