This website provides information on patients with variants in the DALRD3 gene, including clinical data, molecular data, management and research options.

Patients with loss-of-function variants in the DALRD3 gene exhibit clinical symptoms classified as developmental and epileptic encephalopathy disorder (OMIM: #618910). Epileptic encephalopathies are severe epilepsy syndromes characterized by early onset and progressive cerebral dysfunction.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with pathogenic variants in the DALRD3 gene.

Dragony Fu, PhD, University of Rochester, Rochester, NY, USA, dragonyfu@rochester.edu