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[Social cognition disorders in Klinefelter syndrome: A specific phenotype? (KS)]. / Troubles de la cognition sociale dans le syndrome de Klinefelter : un trait phénotypique ?
Babinet, M-N; Rigard, C; Peyroux, É; Dragomir, A-R; Plotton, I; Lejeune, H; Demily, C.
Afiliación
  • Babinet MN; GénoPsy, centre de dépistage et de prises en charge des troubles psychiatriques d'origine génétique, centre hospitalier Le-Vinatier, 95, boulevard Pinel, 69500 Bron, France; EDR-Psy, UMR 5929, CNRS, université Lyon 1, 67, boulevard Pinel, 69500 Bron, France.
  • Rigard C; GénoPsy, centre de dépistage et de prises en charge des troubles psychiatriques d'origine génétique, centre hospitalier Le-Vinatier, 95, boulevard Pinel, 69500 Bron, France; EDR-Psy, UMR 5929, CNRS, université Lyon 1, 67, boulevard Pinel, 69500 Bron, France.
  • Peyroux É; GénoPsy, centre de dépistage et de prises en charge des troubles psychiatriques d'origine génétique, centre hospitalier Le-Vinatier, 95, boulevard Pinel, 69500 Bron, France; EDR-Psy, UMR 5929, CNRS, université Lyon 1, 67, boulevard Pinel, 69500 Bron, France.
  • Dragomir AR; GénoPsy, centre de dépistage et de prises en charge des troubles psychiatriques d'origine génétique, centre hospitalier Le-Vinatier, 95, boulevard Pinel, 69500 Bron, France; EDR-Psy, UMR 5929, CNRS, université Lyon 1, 67, boulevard Pinel, 69500 Bron, France; Service de médecine de la reproduction, l
  • Plotton I; Service de médecine de la reproduction, laboratoire d'hormonologie-endocrinologie moléculaire et maladies rares, hôpital Femme-Mère-Enfant, hospices civils de Lyon, université Lyon 1, 3, quai des Célestins, 69002 Lyon, France.
  • Lejeune H; Service de médecine de la reproduction, laboratoire d'hormonologie-endocrinologie moléculaire et maladies rares, hôpital Femme-Mère-Enfant, hospices civils de Lyon, université Lyon 1, 3, quai des Célestins, 69002 Lyon, France.
  • Demily C; GénoPsy, centre de dépistage et de prises en charge des troubles psychiatriques d'origine génétique, centre hospitalier Le-Vinatier, 95, boulevard Pinel, 69500 Bron, France; EDR-Psy, UMR 5929, CNRS, université Lyon 1, 67, boulevard Pinel, 69500 Bron, France. Electronic address: caroline.demily@ch-le
Encephale ; 43(5): 423-428, 2017 Oct.
Article en Fr | MEDLINE | ID: mdl-27743676
ABSTRACT

INTRODUCTION:

The Klinefelter syndrome (KS) is a genetic condition characterized by an X supernumerary sex chromosome in males. The syndrome is frequently associated with cognitive impairment. Indeed, the different areas of the executive sphere can be affected such as inhibition, cognitive flexibility but also attentional and visual-spatial domain. Social cognition disorders, predominantly on emotional recognition processes, have also been documented. In addition, the syndrome may be associated with psychiatric symptoms. MATERIAL AND

METHOD:

Our study aims to characterize of the various components of social cognition in the SK facial emotional recognition, theory of mind and attributional style. For this two groups (SK group versus control group) of participants (n=16) matched for age and sociocultural level were recruited. Participants with intellectual disabilities, psychiatric or neurological disorders were excluded. Three social cognition tests were available the TREF, the MASC, the AIHQ. Neurocognitive functions were assessed by the fNart, the subtest "logical memory" of the MEM-III, the subtests of the two VOSP battery, the d2, the TMT and the Stroop test.

RESULTS:

The SK group had specific social cognition disorders in comparison to the control group. Two emotions in particular were less well recognized fear and contempt. In addition, the SK group had significantly lower results in theory of mind. Regarding the hostile attribution bias, no significant difference was found. Finally, the results showed correlations between specific attentional disorders and facial emotional recognition. DISCUSSION-

CONCLUSION:

Our study emphasizes social cognition disorders in SK. These disorders could be considered as a phenotypic trait in the syndrome. The interest of better characterizing the cognitive phenotype of genetic disorders that can affect the neurodevelopment is to offer specific cognitive remediation strategies.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Conducta Social / Percepción Social / Cognición / Síndrome de Klinefelter Tipo de estudio: Qualitative_research Límite: Adolescent / Adult / Humans / Male Idioma: Fr Revista: Encephale Año: 2017 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Conducta Social / Percepción Social / Cognición / Síndrome de Klinefelter Tipo de estudio: Qualitative_research Límite: Adolescent / Adult / Humans / Male Idioma: Fr Revista: Encephale Año: 2017 Tipo del documento: Article País de afiliación: Francia