Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skills

Author:

Babinet Marie-Noëlle123,Thomas Nadine1,Pons Linda1,Schluth-Bolard Caroline45,Sanlaville Damien45,Demily Caroline13

Affiliation:

1. Reference Center for Rare Diseases (GénoPsy), Le Vinatier Hospital

2. Unité de Recherche Étude des Mécanismes Cognitifs (EA 3082), Université Lumière Lyon 2, Université de Lyon

3. UMR 5229, CNRS & Université Claude Bernard Lyon 1, Université de Lyon, Institut des Sciences Cognitives Marc Jeannerod, Bron Cedex

4. Genetics Department, GH Est, Hospices Civils de Lyon, Lyon

5. GENDEV Team, CRNL, CNRS UMR 5292, INSERM U1028; Claude Bernard Lyon I University, Lyon, France

Abstract

Rearrangements of 22q11.2 region, most often deletions and duplications, are responsible for multiple congenital disorders. These rearrangements are involved in syndromes that share some phenotypic similarities. To date, 22q11.2 triplication remains very rare, with few cases described in the literature. Here, we report for the first time the clinical, neurocognitive, social cognition and psychiatric properties of a 6-year-old child with 22q11.2 triplication, in comparison with a patient with 22q11.2 duplication and 16 cases of patients with 22q11.2 deletion. Chromosomal region 22q11.2 seems to be a critical locus for sociability and attentional skills and rearrangements could be interpreted as a predisposing factor for the development of psychotic symptoms (22q11.2 deletion), a protective factor (22q11.2 duplication) or a tendency factor for hypersociability (22q11.2 triplication).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics (clinical),Genetics

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