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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...
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| Pubblicato in: | Int J Pediatr Endocrinol |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4890323/ https://ncbi.nlm.nih.gov/pubmed/27257411 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13633-016-0029-3 |
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