Our goal is to connect families of individuals diagnosed with a mutation on the DAGLA gene and diagnosed with NODRS

In June 2022 a study was published for the first time recognizing NODRS (Neuro-Ocular DAGLA Related Syndrome) as a syndrome resulting from a mutation on the DAGLA gene. The common symptoms are ataxia, developmental delays, and nystagmus with a chin tuck. To view this study, please click on the link below.