A rare occurrence of a hereditary Birt-Hogg-Dubé syndrome: A case report

BACKGROUND: Birt-Hogg-Dubé (BHD) syndrome is a rare autosomal dominant disease caused by germline mutations in the folliculin (FLCN) protein gene, which usually manifests as cutaneous fibrofolliculoma, pulmonary cysts, renal cell carcinoma, and spontaneous pneumothorax. CASE SUMMARY: A 26-year-old w...

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Detalles Bibliográficos
Autores principales: Lu, You-Ran, Yuan, Qing, Liu, Jian, Han, Xue, Liu, Min, Liu, Qing-Quan, Wang, Yu-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409184/
https://www.ncbi.nlm.nih.gov/pubmed/34540968
http://dx.doi.org/10.12998/wjcc.v9.i24.7123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409184/
https://www.ncbi.nlm.nih.gov/pubmed/34540968
http://dx.doi.org/10.12998/wjcc.v9.i24.7123

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