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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Eur Clin Respir J
Egile Nagusiak: Jensen, Dea Kejlberg, Villumsen, Anders, Skytte, Anne-Bine, Madsen, Mia Gebauer, Sommerlund, Mette, Bendstrup, Elisabeth
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Taylor & Francis 2017
Gaiak:
Review Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5345590/
https://ncbi.nlm.nih.gov/pubmed/28326182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/20018525.2017.1292378
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