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

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

Abstract Background 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 EHMT1 gene and is characterized by intellectual disability (ID), chi...

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Bibliographic Details
Main Authors: Mengyue Niu, Yanjing Li, Shikun Zhan, Bomin Sun, Jun Liu, Yiwen Wu
Format: Article
Language:English
Published: BMC 2023-10-01
Series:BMC Neurology
Subjects:
Tourette syndrome
Kleefstra syndrome 1
EHMT1 gene
Intellectual disability
Tic disorders
Online Access:https://doi.org/10.1186/s12883-023-03417-x

Internet

https://doi.org/10.1186/s12883-023-03417-x

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