Gilles de la Tourette syndrome as a rare co-morbidity of Klinefelter syndrome.
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.Mots clés
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