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Achondroplasia with 47, xxy karyotype: a case report of the neonatal diagnosis of an extremely unusual association
BACKGROUND: The association of achondroplasia and Klinefelter syndrome is extremely rare. To date, five cases have been previously reported, all of them diagnosed beyond the postnatal period, and only one was molecularly characterized. We describe the first case of this unusual association diagnosed...
Sparad:
| Huvudupphovsmän: | , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2012
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3514257/ https://ncbi.nlm.nih.gov/pubmed/22747519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-12-88 |
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