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Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skills.
Babinet, Marie-Noëlle; Thomas, Nadine; Pons, Linda; Schluth-Bolard, Caroline; Sanlaville, Damien; Demily, Caroline.
Affiliation
  • Babinet MN; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy Lyon), Centre d'excellence autisme iMIND, Centre Hospitalier Le Vinatier, 95 Boulevard Pinel, 69500 Bron, France et UMR 5229, CNRS & Université Lyon 1.
  • Thomas N; Unité de Recherche Étude des Mécanismes Cognitifs, Université Lumière Lyon 2, Université de Lyon, 5 avenue Pierre Mendes-France, 69676 Bron cedex, France.
  • Pons L; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy Lyon), Centre d'excellence autisme iMIND, Centre Hospitalier Le Vinatier, 95 Boulevard Pinel, 69500 Bron, France et UMR 5229, CNRS & Université Lyon 1.
  • Schluth-Bolard C; Centre de Référence Maladies Rares Troubles du Comportement d'Origine Génétique (GénoPsy Lyon), Centre d'excellence autisme iMIND, Centre Hospitalier Le Vinatier, 95 Boulevard Pinel, 69500 Bron, France et UMR 5229, CNRS & Université Lyon 1.
  • Sanlaville D; Unité Fonctionnelle de Cytogénétique, Laboratoire de Biologie Médicale, Centre Hospitalier de Valence, Valence, France.
  • Demily C; Genetics Department, GH Est, Hospices Civils de Lyon, Lyon, France.
Psychiatr Genet ; 33(5): 202-205, 2023 10 01.
Article in En | MEDLINE | ID: mdl-37706496
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).
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / DiGeorge Syndrome Limits: Child / Humans Language: En Journal: Psychiatr Genet Journal subject: GENETICA / PSIQUIATRIA Year: 2023 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / DiGeorge Syndrome Limits: Child / Humans Language: En Journal: Psychiatr Genet Journal subject: GENETICA / PSIQUIATRIA Year: 2023 Document type: Article Country of publication: United kingdom