[Patients with ARHGEF9-mutation: a case report and implications of genetic disorders in child psychiatry]

Tijdschr Psychiatr. 2019;61(12):891-896.
[Article in Dutch]

Abstract

We describe two patients, who were assessed at a child psychiatry clinic, with a known genetic disorder in the ARHGEF9 gene on the long arm of the X chromosome. The boys presented with developmental delay, hyperactivity, autism spectrum disorder and epilepsy. This prompted us to conduct a literature search on previously identified patients with the same mutation and its impact on psychiatric symptoms in children. Recent evolutions in genetic technologies have led to the possibility of identifying and investigating more children with developmental disorders with or without psychiatric disorders. Child psychiatrists are confronted with the question what role genetics play in the child's clinical presentation. A basic knowledge of genetic principles is now required.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Autism Spectrum Disorder / genetics*
  • Child
  • Child Psychiatry*
  • Developmental Disabilities / genetics*
  • Epilepsy / genetics*
  • Humans
  • Male
  • Rho Guanine Nucleotide Exchange Factors

Substances

  • ARHGEF9 protein, human
  • Rho Guanine Nucleotide Exchange Factors