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Recurrent renal cancer in Birt–Hogg–Dubé syndrome: A case report
INTRODUCTION: Birt–Hogg–Dubé syndrome (BHDS) is a rare autosomal dominant disease. It is caused by constitutional mutations in the FLCN gene. Since BHDS is a rare syndrome therefore it is unknown to many physicians. However, it is important to identify this rare syndrome at early stages because inci...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726742/ https://www.ncbi.nlm.nih.gov/pubmed/29223882 http://dx.doi.org/10.1016/j.ijscr.2017.11.032 |