An adolescent with 48,xxyy syndrome with hypergonadotrophic hypogonadism, attention deficit hyperactive disorder and renal malformations

An adolescent with 48,xxyy syndrome with hypergonadotrophic hypogonadism, attention deficit hyperactive disorder and renal malformations

48,XXYY is a rare sex chromosome aneuploidy affecting 1 in 18,000 to 50,000 male births. They present with developmental delay, hypogonadism, gynecomastia, intention tremors, and a spectrum of neurodevelopmental and psychiatric disorders. At one time this condition was considered a variant of Klinef...

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Bibliographic Details
Main Authors: Prasad Katulanda, J. Rasika D. K. Rajapakse, Jayani Kariyawasam, Rohan Jayasekara, Vajira H. W. Dissanayake
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Indian Journal of Endocrinology and Metabolism
Subjects:
48
XXYY syndrome
hypergonadotrophic hypogonadism
sex chromosome aneuploidy
Online Access:http://www.ijem.in/article.asp?issn=2230-8210;year=2012;volume=16;issue=5;spage=824;epage=826;aulast=Katulanda

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http://www.ijem.in/article.asp?issn=2230-8210;year=2012;volume=16;issue=5;spage=824;epage=826;aulast=Katulanda

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