RENOct 4, 20205 minGet To Know The International Foundation for CDKL5 ResearchAbout CDKL5 CDKL5 deficiency disorder (CDD) is a rare developmental epileptic encephalopathy (DEE) caused by mutations in the CDKL5 gene....
RENOct 4, 20205 minGet To Know Ring14 USAAbout Ring14 Ring14 USA supports all neurodevelopmental anomalies on the 14th chromosome, in particular, Ring Chromosome 14 Syndrome....
RENOct 3, 20202 minGet To Know the Angelman Syndrome FoundationAbout Angelman Syndrome (AS) Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births or 500,000...
RENAug 26, 20205 minGet To Know The Cute Syndrome Foundation (SCN8A Epilepsy)About SCN8A SCN8A Epilepsy is a rare developmental epileptic encephalopathy associated with mutations in the gene SCN8A. The first known...
RENJul 31, 20203 minGet To Know SCN2A AUSTRALIAAbout SCN2A SCN2A-related disorders are caused by pathogenic variants in the SCN2A gene on chromosome 2. The SCN2A gene encodes the...