Ontology highlight
ABSTRACT:
SUBMITTER: van Dongen LCM
PROVIDER: S-EPMC7540409 | biostudies-literature | 2020 Oct
REPOSITORIES: biostudies-literature
van Dongen Linde C M LCM Wingbermühle Ellen E Dingemans Alexander J M AJM Bos-Roubos Anja G AG Vermeulen Karlijn K Pop-Purceleanu Monica M Kleefstra Tjitske T Egger Jos I M JIM
American journal of medical genetics. Part A 20200811 10
Witteveen-Kolk syndrome (WITKOS) is a rare neurodevelopmental disorder characterized by developmental delay/intellectual disability, facial dysmorphisms, and short stature. The syndrome is caused by loss of function of switch-insensitive 3 transcription regulator family member A (SIN3A). Regarding behavioral functioning, Autism Spectrum Disorders (ASD), obsessive-compulsive behaviors, as well as Attention-Deficit/Hyperactivity Disorder symptoms (ADHD) have been suggested. The present study explo ...[more]