Disorder of Sexual Development and Congenital Heart Defect in 47XYY: Clinical Disorder or Coincidence?

Background. 47XYY syndrome is a rare sex chromosome variation characterized by an additional Y chromosome. Most patients with 47XYY karyotype have normal phenotype. This disorder seems associated with a higher risk of developing behavioral and cognitive problems, tall stature, and infertility in adu...

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Detalles Bibliográficos
Autores principales: Latrech, Hanane, Skikar, Imane, Gharbi, Mohammed El Hassan, Chraïbi, Abdelmjid, Gaouzi, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484839/
https://www.ncbi.nlm.nih.gov/pubmed/26175918
http://dx.doi.org/10.1155/2015/802162

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484839/
https://www.ncbi.nlm.nih.gov/pubmed/26175918
http://dx.doi.org/10.1155/2015/802162

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