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A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome
BACKGROUND: 47 XXY/46 XX mosaicism with characteristics suggesting Klinefelter syndrome is very rare and at present, only seven cases have been reported in the literature. CASE PRESENTATION: We report an Indian boy diagnosed as variant of Klinefelter syndrome with 47 XXY/46 XX mosaicism at age 12 ye...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890323/ https://www.ncbi.nlm.nih.gov/pubmed/27257411 http://dx.doi.org/10.1186/s13633-016-0029-3 |