Tourette-like syndrome secondary to Kleefstra syndrome 1 with a de novo microdeletion in the EHMT1 gene

Gills de la Tourette syndrome (TS) is a childhood-onset neurodevelopmental disorder manifested by motor and vocal tics. Kleefstra syndrome 1 (KS1), a rare genetic disorder, is caused by haploinsufficiency of the

Source: BMC Neurology - October 10, 2023 Category: Neurology Authors: Mengyue Niu, Yanjing Li, Shikun Zhan, Bomin Sun, Jun Liu and Yiwen Wu Tags: Case Report Source Type: research