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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Detalles Bibliográficos
Autores principales: Katulanda, Prasad, Rajapakse, J. Rasika D. K., Kariyawasam, Jayani, Jayasekara, Rohan, Dissanayake, Vajira H. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475914/
https://www.ncbi.nlm.nih.gov/pubmed/23087874
http://dx.doi.org/10.4103/2230-8210.100642

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475914/
https://www.ncbi.nlm.nih.gov/pubmed/23087874
http://dx.doi.org/10.4103/2230-8210.100642

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