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Rare 48, XYYY syndrome: case report and review of the literature
48, XYYY syndrome is a rare condition. A male with 32‐year‐old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi‐Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity...
Sparad:
| I publikationen: | Clin Case Rep |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
John Wiley and Sons Inc.
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5771943/ https://ncbi.nlm.nih.gov/pubmed/29375860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1311 |
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