Psychosis and autism without functional regression in a patient with Kleefstra syndrome

Psychiatr Genet. 2023 Feb 1;33(1):34-36. doi: 10.1097/YPG.0000000000000330. Epub 2022 Dec 1.

Abstract

Kleefstra syndrome is a rare genetic disorder caused by haploinsufficiency of the euchromatic histone lysine methyltransferase 1 (EHMT1) gene. It is characterized by a variety of dysmorphic features, comorbid medical issues, and developmental delays/intellectual disability. Neuropsychiatric symptoms may also occur, including autistic features and psychosis, and are often accompanied by functional regression. However, the phenomenology of psychotic symptoms in this syndrome has not been well described in the literature. As such, in this brief report, we review the literature with respect to the occurrence of psychosis in Kleefstra syndrome and describe the symptom profile of a 35-year-old affected male with an intellectual disability, autism spectrum disorder, and schizophrenia (in association with manic features). This is the first report of psychotic symptoms fully remitting in response to zuclopenthixol therapy in an individual with Kleefstra syndrome. This case is also unique as it demonstrates that functional regression does not necessarily coincide with the development of schizophrenia-like presentations in affected individuals.

Publication types

  • Review

MeSH terms

  • Adult
  • Autism Spectrum Disorder* / genetics
  • Autistic Disorder* / genetics
  • Chromosome Deletion
  • Chromosomes, Human, Pair 9
  • Craniofacial Abnormalities
  • Heart Defects, Congenital
  • Humans
  • Intellectual Disability* / genetics
  • Male
  • Psychotic Disorders* / complications
  • Psychotic Disorders* / genetics

Supplementary concepts

  • Kleefstra Syndrome