Oral and maxillo-facial manifestations of systemic diseases: an overview

S Capodiferro, L Limongelli, G Favia - Medicina, 2021 - mdpi.com
Many systemic (infective, genetic, autoimmune, neoplastic) diseases may involve the oral
cavity and, more generally, the soft and hard tissues of the head and neck as primary or …

[HTML][HTML] Aporte de la radiología oral y maxilofacial al diagnóstico clínico

C Paz Gallardo, C Celis Contreras… - Avances en …, 2019 - SciELO Espana
Introducción La radiología oral y maxilofacial (RMF) es la disciplina encargada del uso de
rayos X y otros tipos de radiación para el diagnóstico de enfermedades y condiciones del …

Osteoma of the jaw as first clinical sign of Gardner's syndrome: the experience of two Italian centers and review

S D'Agostino, F Dell'Olio, A Tempesta… - Journal of clinical …, 2023 - mdpi.com
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 …

Gardner syndrome with maxillofacial manifestation: A case report

ME Baldino, VS Koth, DN Silva… - Special Care in …, 2019 - Wiley Online Library
Gardner syndrome is a hereditary disease in which patients develop gastrointestinal polyps,
osteomas, desmoid tumors, epidermoid cysts, fibromas, lipomas, and retinal lesions. Dental …

Public attitudes toward chairside screening for medical conditions in dental settings

A Bin Mubayrik, S Al Dosary, R Alshawaf… - Patient preference …, 2021 - Taylor & Francis
Objective The aim of this study is to investigate the public's attitudes and knowledge toward
chairside dental screening and laboratory investigations based on demographic data …

[PDF][PDF] Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early …

G Antal, A Zsigmond, Á Till, E Orsi, I Szanto… - Pathology and …, 2024 - por-journal.com
Background: Gardner syndrome is a rare genetic cancer predisposition disorder
characterized by intestinal polyposis, multiple osteomas, and soft and hard tissue tumors …

APC c.4621C>T variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism

D Cai, F He, X Xu, F Xiong… - Experimental and …, 2021 - spandidos-publications.com
Gardner's syndrome is a rare autosomal dominant hereditary disease that is characterized
by multiple colorectal polyps combined with extra‑colonic presentation (such as osteoma or …

[PDF][PDF] A Case of Early FAP Diagnosis with Extraintestinal Manifestations on the Face.

V Thomaidis, K Seretis, G Tsoucalas… - Acta Medica …, 2019 - researchgate.net
Objective. Gardner's syndrome is a variant of familial adenomatous polyposis, characterized
by gastrointestinal polyps, multiple osteomas, and skin and soft tissue lesions. Diagnosis by …

Los recursos informáticos en las especialidades de estomatología y cirugía maxilofacial desde una perspectiva de ciencia, tecnología y sociedad

A Soto Ugalde, B Mesa Reynaldo - Revista Universidad y Sociedad, 2023 - scielo.sld.cu
El presente trabajo hace una valoración critica del estado de los recursos informáticos en la
especialidad de estomatología y cirugía maxilofacial, utilizando una visión de ciencia …

SÍNDROME DE GARDNER: IMPORTÂNCIA DO CIRURGIÃO-DENTISTA NO DIAGNOSTICO PRECOCE DE UMA LESÃO POTENCIALMENTE FATAL: REVISÃO DE …

PE PONTES MEDEIROS… - Brazilian Journal of …, 2022 - search.ebscohost.com
RESUMO A síndrome de Gardner (SG) é uma doença hereditária, de característica
autossômica dominante que foi causada a partir de uma mutação do gene adenomatous …