Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2)

Wendy R. Kates, Courtney P. Burnette, Brandy A. Bessette, Bradley S. Folley, Leslie Strunge, Ethylin Jabs, Godfrey D. Pearlson

Research output: Contribution to journalArticle

Abstract

This study investigated the morphology of the frontal lobe and the caudate nucleus in velocardiofacial syndrome, a neurogenetic disorder caused by a microdeletion at chromosome 22q11.2 and frequently associated with severe psychiatric disturbances. Volumes of the caudate nucleus and subregions of the frontal lobe were compared on magnetic resonance images of 10 children with velocardiofacial syndrome and 10 age- and gender-matched controls. Frontal deep white matter was reduced significantly (by about 23%) in subjects with velocardiofacial syndrome relative to controls. Frontal and pre-frontal volumes were also reduced in subjects with velocardiofacial syndrome, although not disproportionately to whole brain volume. The volume of the right caudate nucleus was increased in children with velocardiofacial syndrome. Associations between right caudate and right frontal regions were noted in controls but not in children with velocardiofacial syndrome. These findings suggest frontostriatal dysfunction in children with velocardiofacial syndrome. Insofar as up to 30% of adults with velocardiofacial syndrome (also known as chromosome 22q11 deletion syndrome) develop schizophrenia and frontostriatal dysfunction has been noted in schizophrenia, the findings support the hypothesis that velocardiofacial syndrome might represent a neurodevelopmental model of schizophrenia.

Original languageEnglish (US)
Pages (from-to)337-342
Number of pages6
JournalJournal of child neurology
Volume19
Issue number5
DOIs
StatePublished - May 2004
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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  • Cite this

    Kates, W. R., Burnette, C. P., Bessette, B. A., Folley, B. S., Strunge, L., Jabs, E., & Pearlson, G. D. (2004). Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2). Journal of child neurology, 19(5), 337-342. https://doi.org/10.1177/088307380401900506