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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Hindawi Publishing Corporation
2015
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| Materias: | |
| 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 |