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Co-occurrence of Marfan syndrome and schizophrenia: what can be learned?

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

We report on a young female patient diagnosed with Marfan syndrome upon admission to the psychiatric hospital for a first psychosis. Mutation analysis of FBN1 identified a de novo nonsense mutation (p.Glu178X). This finding implies co-occurrence of schizophrenia and Marfan syndrome, an observation that has been reported several times in the past. Although, this co-occurrence can be coincidental, several arguments provide strong evidence that Marfan syndrome and schizophrenia might share common etiological pathways. This observation can be important in light of both the etiology of schizophrenia and the diagnosis of Marfan syndrome.

Original languageEnglish
Pages (from-to)252-5
Number of pages4
JournalEuropean Journal of Medical Genetics
Volume55
Issue number4
DOIs
Publication statusPublished - Apr 2012
Externally publishedYes

Keywords

  • Codon, Nonsense
  • DNA Mutational Analysis
  • Female
  • Fibrillin-1
  • Fibrillins
  • Genotype
  • Humans
  • Marfan Syndrome/complications
  • Microfilament Proteins/genetics
  • Pedigree
  • Phenotype
  • Schizophrenia/complications
  • Young Adult
  • Adipokines

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