{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,29]],"date-time":"2026-07-29T22:52:46Z","timestamp":1785365566659,"version":"3.55.0"},"reference-count":14,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2016,9,19]],"date-time":"2016-09-19T00:00:00Z","timestamp":1474243200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2016,12]]},"abstract":"<jats:sec><jats:label\/><jats:p>Birt\u2013Hogg\u2013Dube syndrome (BHD) is an autosomal dominant disease characterised by benign cutaneous lesions, pulmonary cysts, and an increased risk of renal tumors. This rare condition is due to a mutation in the folliculin (<jats:italic>FLCN<\/jats:italic>) gene on chromosome 17q11.2, which has a role in the mechanistic\/mammalian target of rapamycin (mTOR) signaling pathway of tumorigenesis. This case illustrates a patient with BHD and a renal angiomyolipoma, a neoplastic lesion not usually associated with BHD but common in Tuberous Sclerosis Complex (TSC). There is both clinical and molecular overlap between BHD and TSC, which may arise from similarities in function of the TSC and FLCN proteins in the mTOR pathway; this case further demonstrates this potential correlation. \u00a9 2016 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.37952","type":"journal-article","created":{"date-parts":[[2016,9,19]],"date-time":"2016-09-19T13:33:50Z","timestamp":1474292030000},"page":"3323-3326","source":"Crossref","is-referenced-by-count":12,"title":["Renal angiomyolipoma in Birt\u2013Hogg\u2013Dube syndrome: A case study supporting overlap with tuberous sclerosis complex"],"prefix":"10.1002","volume":"170","author":[{"given":"Eryn","family":"Dow","sequence":"first","affiliation":[{"name":"Genetic Medicine and Family Cancer Clinic Royal Melbourne Hospital Melbourne Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ingrid","family":"Winship","sequence":"additional","affiliation":[{"name":"Genetic Medicine and Family Cancer Clinic Royal Melbourne Hospital Melbourne Victoria Australia"},{"name":"Department of Medicine University of Melbourne Parkville Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2016,9,19]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.36917"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1440-0960.2011.00738.x"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1111\/iju.13015"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddp032"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1038\/modpathol.3880275"},{"key":"e_1_2_4_7_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2133.2009.09517.x"},{"key":"e_1_2_4_8_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2230.2008.03065.x"},{"key":"e_1_2_4_9_1","first-page":"382","article-title":"Birt\u2010Hogg\u2010Dube (BHD) syndrome: Report of two novel germline mutations in the folliculin (FLCN) gene","volume":"18","author":"Palmirotta R","year":"2008","journal-title":"Eur J Dermatol"},{"key":"e_1_2_4_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.crad.2005.01.009"},{"key":"e_1_2_4_11_1","doi-asserted-by":"publisher","DOI":"10.1097\/01.ju.0000154629.45832.30"},{"key":"e_1_2_4_12_1","doi-asserted-by":"publisher","DOI":"10.2169\/internalmedicine.51.7211"},{"key":"e_1_2_4_13_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.2007.054304"},{"key":"e_1_2_4_14_1","doi-asserted-by":"publisher","DOI":"10.1158\/1078-0432.CCR-08-0608"},{"key":"e_1_2_4_15_1","first-page":"393","article-title":"Risk of renal and colonic neoplasm and spontaneous pneumothorax in the Birt\u2010Hogg\u2010Dube syndrome","volume":"11","author":"Zbar B","year":"2001","journal-title":"Cancer Epidemiol"}],"container-title":["American Journal of Medical Genetics Part A"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.a.37952","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.a.37952","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.a.37952","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,7]],"date-time":"2023-10-07T01:40:43Z","timestamp":1696642843000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.a.37952"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,9,19]]},"references-count":14,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2016,12]]}},"alternative-id":["10.1002\/ajmg.a.37952"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.a.37952","archive":["Portico"],"relation":{},"ISSN":["1552-4825","1552-4833"],"issn-type":[{"value":"1552-4825","type":"print"},{"value":"1552-4833","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,9,19]]}}}