Birt–Hogg–Dubé syndrome: a case report and a review of the literature

Background: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant inherited syndrome caused by mutations in the folliculin coding gene (FLCN). The clinical manifestations of the syndrome involve the skin, lungs, and kidneys. Because of the rarity of the syndrome, guidelines for diagnosis and m...

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Detalles Bibliográficos
Autores principales: Jensen, Dea Kejlberg, Villumsen, Anders, Skytte, Anne-Bine, Madsen, Mia Gebauer, Sommerlund, Mette, Bendstrup, Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345590/
https://www.ncbi.nlm.nih.gov/pubmed/28326182
http://dx.doi.org/10.1080/20018525.2017.1292378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345590/
https://www.ncbi.nlm.nih.gov/pubmed/28326182
http://dx.doi.org/10.1080/20018525.2017.1292378

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