Birt-Hogg-Dube syndrome prospectively detected by review of chest computed tomography scans

PURPOSE: Birt-Hogg-Dube syndrome (BHD) is a rare disorder caused by mutations in the gene that encodes folliculin (FLCN) and is inherited in an autosomal dominant manner. BHD is commonly accompanied by fibrofolliculomas, renal tumors, multiple pulmonary cysts, and spontaneous pneumothorax. The aim o...

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Detalles Bibliográficos
Autores principales: Park, Hye Jung, Park, Chul Hwan, Lee, Sang Eun, Lee, Geun Dong, Byun, Min Kwang, Lee, Sungsoo, Lee, Kyung-A, Kim, Tae Hoon, Kim, Seong Han, Yang, Seo Yeon, Kim, Hyung Jung, Ahn, Chul Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289479/
https://www.ncbi.nlm.nih.gov/pubmed/28151982
http://dx.doi.org/10.1371/journal.pone.0170713

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289479/
https://www.ncbi.nlm.nih.gov/pubmed/28151982
http://dx.doi.org/10.1371/journal.pone.0170713

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