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A rare sex chromosome aneuploidy: 48,XXYY syndrome
48,XXYY syndrome is a rare sex chromosome abnormality. Although some physical features are similar to Klinefelter syndrome(47,XXY), 48,XXYY is typically associated with different neuropsyhciatric symptoms and phenotypic findings. Approximately 100 cases with 48,XXYY have been reported to date. In th...
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| Publicado en: | Turk Pediatri Ars |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Turkish Pediatrics Association
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4959738/ https://ncbi.nlm.nih.gov/pubmed/27489468 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2016.1551 |
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