Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response

Marco Fichera, Rita Barone, Lucia Grillo, Mariaclara De Grandi, Valerio Fiore, Ignazio Morana, Tiziana Maniscalchi, Mirella Vinci, Silvestra Amata, Angela Spalletta, Giovanni Sorge, Salvatore Santo Signorelli

Research output: Contribution to journalArticle

Abstract

Background: Despite the extensive use of chromosomal microarray technologies in patients with neurodevelopmental disorders has permitted the identification of an increasing number of causative submicroscopic rearrangements throughout the genome, constitutional duplications involving chromosome 1q22 have seldom been described in those patients. Results: We report on a pedigree with seven affected members showing varying degrees of behavioural and emotional disturbances including general anxiety disorder, mood disorders, and intellectual disability. Two adult female patients also showed late onset autoimmune inflammatory responses characterized by alopecia, skin ulcers secondary to inflammatory vasculitis, interstitial lung disease, and Raynaud's phenomenon. Array-CGH analysis identified in the affected individuals a 290 Kb microduplication in the chromosome 1q22. The rearrangement involves eleven known genes and is not present in the databases of polymorphic copy number variants. Conclusions: The rearrangement segregates with the neurological clinical features observed in our patients, suggesting that dosage imbalance of one or more genes in this genomic region may lead to the observed phenotype. The association between the microduplication and the inflammatory disease is much less evident. Additional reported patients carrying similar microduplications are needed to clarify this aspect.

Original languageEnglish
Article number90
JournalMolecular Cytogenetics
Volume7
Issue number1
DOIs
Publication statusPublished - 2014

Keywords

  • 1q22
  • CBCL dysregulation syndrome
  • CNV
  • Duplication
  • Inflammatory disease
  • Intellectual disability
  • LAMTOR2
  • LMNA
  • SEMA4A

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Biochemistry, medical

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