APC is a tumor suppressor gene that exerts its effect through the regulation of the Wnt
signaling pathway. Loss of function mutations of the gene are associated with familial …

Cancer predisposition syndromes are entities determined especially by germinal pathogenic
variants, with most of them autosomal dominantly inherited. The risk of a form of cancer is …

Gardner's syndrome (GS) is a combination of polyposis, osteomas, fibromas, and sebaceous
cysts. The aim of the study is to highlight whether maxillofacial osteoma could represent an …

Objectives: Identify the etiology of Gardner syndrome. Describe the typical presentation of a
patient with Gardner syndrome. Outline the treatment and management options available for …

This review article focuses on the various primary osseous tumors of the orbit. Due to
overlapping clinical, radiologic, and histologic features, differentiating these entities can …

Background Hereditary adenomatous polyposis syndromes, including familial adenomatous
polyposis and other rare adenomatous polyposis syndromes, increase the lifetime risk of …

Familial adenomatous polyposis (FAP) is an autosomal dominant colorectal cancer
syndrome that is characterized by the development of multiple adenomas in the colon and …

Gardner syndrome (GS) is a specific form of familial adenomatous polyposis (FAP), which
manifests as colorectal polyps, multiple osteomas and soft tissue tumors, and in the oral …

Background: Maxillary sinus augmentation is a method extensively used to restore sufficient
bone volume in the posterior maxilla to allow for the placement of fixtures. The purpose of …

A Síndrome de Gardner, subtipo da Polipose Adenomatosa Familiar, é uma doença
hereditária rara com múltiplos pólipos intestinais e diversas manifestações extraintestinais …