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Concurrent Van der Woude syndrome and Turner syndrome: A case report
Most cases of Van der Woude syndrome are caused by a mutation to interferon regulatory factor 6 on chromosome 1. Turner syndrome is caused by complete or partial absence of the second sex chromosome in girls. We describe a unique case of the two syndromes occurring concurrently though apparently ind...
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| Publicado no: | SAGE Open Med Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5308529/ https://ncbi.nlm.nih.gov/pubmed/28228961 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X16687916 |
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