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Gilles de la Tourette syndrome as a rare co-morbidity of Klinefelter syndrome.
Cavanna, Andrea E; Paini, Giulia; Purpura, Giulia; Riva, Anna; Nacinovich, Renata; Seri, Stefano.
Affiliation
  • Cavanna AE; Department of Neuropsychiatry, BSMHFT and University of Birmingham, Birmingham, UK. a.e.cavanna@bham.ac.uk.
  • Paini G; Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, London, UK. a.e.cavanna@bham.ac.uk.
  • Purpura G; School of Health and Life Sciences, Aston Institute of Health and Neurodevelopment, Aston University, Birmingham, UK. a.e.cavanna@bham.ac.uk.
  • Riva A; School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy. a.e.cavanna@bham.ac.uk.
  • Nacinovich R; Department of Neuropsychiatry, National Centre for Mental Health, 25 Vincent Drive, Birmingham, B15 2FG, UK. a.e.cavanna@bham.ac.uk.
  • Seri S; School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.
Neurol Sci ; 45(8): 4033-4035, 2024 Aug.
Article de En | MEDLINE | ID: mdl-38714596
ABSTRACT

BACKGROUND:

Klinefelter syndrome (47, XXY) is the most common sex chromosome aneuploidy. In addition to male hypergonadotropic hypogonadism, a wide range of neurodevelopmental disorders, anxiety and affective symptoms have been reported in a substantial proportion of cases. CASE DESCRIPTION We document the rare case of a 43-year-old man diagnosed with Klinefelter syndrome and co-morbid Gilles de la Tourette syndrome. He presented with multiple motor and vocal tics since adolescence, as well as anxiety and affective symptoms as his main tic-exacerbating factors. Tic severity was rated as marked (Yale Global Tic Severity Scale score of 78/100), and recommendations for the treatment of both tics and psychiatric co-morbidities were formulated.

DISCUSSION:

Neurodevelopmental tics in the context of Klinefelter syndrome have been previously documented in three cases only. Gilles de la Tourette syndrome is 3-4 times more common in males than females and its etiological factors include multiple genetic components (genetic heterogeneity). Our case report widens the spectrum of neurodevelopmental disorders observed in the context of Klinefelter syndrome and contributes to genetic research on the role of the X chromosome in the pathophysiology of tic disorders.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome de Tourette / Comorbidité / Syndrome de Klinefelter Limites: Adult / Humans / Male Langue: En Journal: Neurol Sci Sujet du journal: NEUROLOGIA Année: 2024 Type de document: Article Pays de publication: Italie

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome de Tourette / Comorbidité / Syndrome de Klinefelter Limites: Adult / Humans / Male Langue: En Journal: Neurol Sci Sujet du journal: NEUROLOGIA Année: 2024 Type de document: Article Pays de publication: Italie