Neurodevelopmental disorders caused by variants in TRPM3

Developmental and epileptic encephalopathies (DEE) are a broad and varied group of disorders that affect the brain and are characterized by epilepsy and comorbid intellectual disability (ID). These conditions have a broad spectrum of symptoms and can be caused by various underlying factors, including genetic mutations, infections, and other medical conditions. The exact cause of DEE remains largely unknown in the majority of cases. However, in around 25 % of patients, rare nonsynonymous coding variants in genes encoding ion channels, cell-surface receptors, and other neuronally expressed proteins are identified. This review focuses on a subgroup of DEE patients carrying variations in the gene encoding the Transient Receptor Potential Melastatin 3 (TRPM3) ion channel, where recent data indicate that gain-of-function of TRPM3 channel activity underlies a spectrum of dominant neurodevelopmental disorders. •Developmental and epileptic encephalopathies (DEE) is a neurodevelopmental disease characterized by intellectual disability and comorbid epilepsy.•TRPM3 is a Ca2+ - permeable cation channel highly expressed in the central nervous system.•De novo TRPM3 variants have been linked to DEE.•Gain-of-function of TRPM3 channel activity underlies a spectrum of dominant neurodevelopmental disorders.