| Literature DB >> 19320655 |
I Kluijt1, D de Jong, H J Teertstra, P H Axwijk, J J P Gille, K Bell, A van Rens, A W G van der Velden, L Middelton, S Horenblas.
Abstract
Birt-Hogg-Dubé syndrome is a hereditary syndrome characterized by benign disease of skin and lungs and a risk of malignant renal tumors. We describe a clinical and genetic study of a large Dutch family with a novel mutation in the FLCN gene. Renal cancer at very young age occurred in one branch of this family, while in other branches, cutaneous and pulmonary symptoms predominated. A variety of congenital anomalies and connective tissue abnormalities were observed, possibly associated with the gene mutation.Entities:
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Year: 2009 PMID: 19320655 DOI: 10.1111/j.1399-0004.2009.01159.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438