DRPLA is a rare and devastating condition. Our son was diagnosed in August 2018. We have developed this webpage to try to find other people who have this condition.
Our goal is to develop a confidential database to share information about drugs and therapy, in particular, and any treatments that have been found to be successful in postponing or lessening symptoms.
In order to do this, we are utilizing a very helpful site called Rare Connect.
This site was established to help families with rare conditions connect and we have set up a subgroup called DRPLA on this page. We would be so grateful if you could register with the DRPLA subgroup.