@article {44038,
	title = {Gardner{\textquoteright}s syndrome: a case report and review of the literature.},
	journal = {World J Gastroenterol},
	volume = {11},
	year = {2005},
	month = {2005 Sep 14},
	pages = {5408-11},
	abstract = {Gardner{\textquoteright}s syndrome is an autosomal dominant disease characterized by the presence of colonic polyposis, osteomas and a multitude of soft tissue tumors. The syndrome may present at any age from 2 mo to 70 years with a variety of symptoms, either colonic or extracolonic. We present a case of a 11-year-old female patient with Gardner{\textquoteright}s syndrome who presented with a lumbar area desmoid tumor and treated with resection of the desmoid, restorative proctocolectomy and ileal pouch anal anastomosis, A review of the current literature has been performed.},
	keywords = {Child, Colonic Pouches, Desmoid Tumors, Female, Gardner Syndrome, Humans, Proctocolectomy, Restorative},
	issn = {1007-9327},
	doi = {10.3748/wjg.v11.i34.5408},
	author = {Fotiadis, C and Tsekouras, D-K and Antonakis, P and Sfiniadakis, J and Genetzakis, M and Zografos, G-C}
}
