European Journal of Dermatology
MENUBirt-Hogg-Dubé (BHD) syndrome: report of two novel germline mutations in the folliculin (FLCN) gene Volume 18, numéro 4, July-August 2008
Illustrations
Raffaele Palmirotta, Pietro Donati, Annalisa Savonarola, Carlo Cota, Patrizia Ferroni, Fiorella Guadagni
Department of Laboratory Medicine & Advanced Biotechnologies, IRCCS San Raffaele Pisana, Via della Pisana 235, 00163 Rome, Italy, Unit of Skin Histopathology, IRCCS San Gallicano Dermatologic Institute, Via E. Chianesi 53, 00144, Rome, Italy
- Mots-clés : Birt-Hogg-Dubé syndrome, cancer predisposition, molecular analysis, mutation, sequence variants
- DOI : 10.1684/ejd.2008.0431
- Page(s) : 382-6
- Année de parution : 2008
Molecular analysis of the folliculin (FLCN) gene was performed in four consenting patients from two families with Birt-Hogg-Dubé (BHD) syndrome, showing the occurrence of two frameshift mutations located respectively in exons 5 (802insA) and 9 (1345delAAAG) of the FLCN gene. A novel homozygous sequence variant in the intron 9 (IVS9 +5C>T) was also found. 1345delAAAG was associated with a wide variety of tumors, including stomach, colon, breast and parotid cancer. Conversely, the family carrying 802insA only had clinical evidence of dermatological lesions. These findings further suggest the relevance of exon 9 mutations in cancer predisposition for BHD.