We report the case of a 12.4 year-old boy who presented Klinefelter Syndrome (KS) mosaicism (46,XY/47,XXY), associated with Mental Retardation and Anorexia Nervosa. KS was undiagnosed before hospitalization in a psychiatric unit. The patient was referred to a child psychiatric unit for restrictive eating. The medical history showed long standing feeding difficulties and failure to thrive. The patient was prebubertal and other clinical characteristics were: microcephaly, short stature and dysmorphic traits. Cytogenetic analysis revealed a mosaicism, 46,XY[11] and 47,XXY[19] karyotype. The psychiatric assessment demonstrated the presence of Anorexia Nervosa and low mood. No specific pathophysiological links between the alterations of KS and the development of anorexia nervosa should be hypothesized on the basis of this Case Report. In prepubertal boys with mental disorders the possibility of KS should be considered, independently of the presence of eating disorders. Nevertheless, the case shows that a KS can be first detected during an assessment for eating disorders. Few cases of the association of KS with AN have been previously reported in literature. This is the first description of a Klinefelter Syndrome, mosaicism (46,XY/47,XXY), associated with Anorexia Nervosa and Mental Retardation. This Case Report illustrates the need, for clinicians who work with Eating Disorders to investigate the possible association between AN and KS, a rare but intriguing one

A case of Klinefelter Syndrome, mosaicism (46,XY/47,XXY), associated with Anorexia Nervosa

GRITTI, Antonella;
2011-01-01

Abstract

We report the case of a 12.4 year-old boy who presented Klinefelter Syndrome (KS) mosaicism (46,XY/47,XXY), associated with Mental Retardation and Anorexia Nervosa. KS was undiagnosed before hospitalization in a psychiatric unit. The patient was referred to a child psychiatric unit for restrictive eating. The medical history showed long standing feeding difficulties and failure to thrive. The patient was prebubertal and other clinical characteristics were: microcephaly, short stature and dysmorphic traits. Cytogenetic analysis revealed a mosaicism, 46,XY[11] and 47,XXY[19] karyotype. The psychiatric assessment demonstrated the presence of Anorexia Nervosa and low mood. No specific pathophysiological links between the alterations of KS and the development of anorexia nervosa should be hypothesized on the basis of this Case Report. In prepubertal boys with mental disorders the possibility of KS should be considered, independently of the presence of eating disorders. Nevertheless, the case shows that a KS can be first detected during an assessment for eating disorders. Few cases of the association of KS with AN have been previously reported in literature. This is the first description of a Klinefelter Syndrome, mosaicism (46,XY/47,XXY), associated with Anorexia Nervosa and Mental Retardation. This Case Report illustrates the need, for clinicians who work with Eating Disorders to investigate the possible association between AN and KS, a rare but intriguing one
2011
Anorexia Nervosa; Klinefelter Syndrome; Child Psychiatry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12570/2329
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