The Kleefstra Syndrome Market is witnessing steady growth as awareness of rare genetic and neurodevelopmental disorders continues to increase and diagnostic capabilities improve worldwide. Kleefstra syndrome is a rare genetic condition caused by mutations or deletions of the EHMT1 gene and is characterized by intellectual disability, hypotonia, delayed speech development, behavioral c... https://www.databridgemarketresearch.com/reports/global-kleefstra-syndrome-market