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Title: [Birt-Hogg-Dubé syndrome]. Author: Křepelová A, Puchmajerová A, Vasovčák P, Chocholatý M. Journal: Klin Onkol; 2012; 25 Suppl():S18-20. PubMed ID: 22920201. Abstract: Birt-Hogg-Dubé syndrome (BHDS, MIM 135150) is an autosomal dominant condition characterized by presence of skin fibrofolliculomas, lung cysts, spontaneous pneumothorax and renal cancer. The disease is caused by germ-line mutations of the FLCN gene, which encodes protein folliculin. BHDS is a rare condition with high penetrance and variable expression. Clinical recommendations include increased care during general anesthesia due to a higher risk of pneumothorax, and long-term follow-up due to an elevated risk of renal cancer. Diagnostic and predictive DNA tests are available; prenatal and preimplantation diagnosis is possible.[Abstract] [Full Text] [Related] [New Search]