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A unique association of Noonan syndrome and 47,XYY syndrome in a male presenting with failure to thrive
We describe a 24-month-old male patient who presented to our Genetics-Endocrinology Clinic with a history of failure to thrive, short stature and cryptorchidism. Soon after birth he was diagnosed with 47,XYY syndrome, but due unusual facial features had further diagnostic workup which revealed Noona...
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| Publicat a: | Oxf Med Case Reports |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5597878/ https://ncbi.nlm.nih.gov/pubmed/28928975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omx032 |
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