Coffin-Lowry Syndrome (CLS)

Coffin-Lowry Syndrome, also known as cls, is related to intellectual developmental disorder, x-linked 19 and symptomatic form of coffin-lowry syndrome in female carriers, and has symptoms including seizures An important gene associated with Coffin-Lowry Syndrome is RPS6KA3 (Ribosomal Protein S6 Kinase A3), and among its related pathways/superpathways are Innate Immune System and Apoptotic Pathways in Synovial Fibroblasts. Affiliated tissues include skeletal muscle and cerebellum, and related phenotypes are intellectual disability and frontal bossing