Results 41 to 50 of about 6,482 (204)

Prevalence of Exostosis in Maxillary Sinus by Cone-Beam Computed Tomography Technique in a Population of Northern Iran [PDF]

Journal of Mashhad Dental School
Background: Antral exostosis in the maxillary sinus generally causes changes in the sinus, and its expansion may complicate planned sinus lift procedures before implant placement in the edentulous posterior maxilla.
Kasra Pishkar, Hakimeh Ghorbani, Farida Abesi, alireza babaeiDarzi, hemmat gholinia   +4 more
doaj   +1 more source

Exposición espontánea de un torus palatino de la línea media

Biomédica: revista del Instituto Nacional de Salud, 2013
Introducción. El torus, o rodete, palatino es una alteración ósea benigna que puede generar molestias en la fonación y en la deglución. Cuando su crecimiento o exposición persistente producen síntomas molestos, debe ser resecado quirúrgicamente ...
Gustavo Sinisterra, Jaime Álvarez, Pablo Emilio Molano   +2 more
doaj   +1 more source

Clinical and radiological characteristics of forearm deformities in children with multiple hereditary exostoses [PDF]

Гений oртопедии, 2019
Introduction The incidence of forearm deformities in children with multiple hereditary exostoses (MHE) ranges from 30 to 80 %. There are few studies of deformities of the forearm in MHE patients in the literature that describe not only the location of ...
Ekaterina A. Zakharyan, Ekaterina A. Belousova, Alexander P. Pozdeev   +2 more
doaj   +1 more source

Exostoses in obturator foramen — an osteological study

Folia Morphologica
BACKGROUND: The obturator foramen is an oval or round opening in the lateral pelvic bone and is normally closed by the obturator membrane, a connective tissue membrane.
Svenja Ebner, Michael J. Schmeisser, Sven Schumann   +2 more
doaj   +1 more source

Multiple Maxillar Exostosis

Journal of the Belgian Society of Radiology, 2019
Teaching point: Multiple buccal exostosis are rare but asymptomatic, unequivocal, and always benign conditions of the ...
Brice Dion, Bruno Coulier
doaj   +1 more source

Forearm deformities in children with hereditary multiple exostosis (review of literature) [PDF]

Гений oртопедии, 2020
Introduction Hereditary multiple exostoses, according to different authors, account for 16.0 to 43.0 % of all the cases of tumors, tumor-like and dysplastic diseases of the pediatric skeleton.
Alexander P. Pozdeev, Ekaterina A. Belousova, Olga N. Sosnenko   +2 more
doaj   +1 more source

Three Novel EXT1 and EXT2 Gene Mutations in Taiwanese Patients with Multiple Exostoses

Journal of the Formosan Medical Association, 2006
Multiple osteochondromatosis, also known as hereditary multiple exostoses (HME), is an inherited autoso-mal dominant disorder characterized by the presence of multiple exostoses on the long bones.
Wen-Chau Chen, Chih-Hsien Chi, Chia-Chang Chuang, l-Ming Jou   +3 more
doaj   +1 more source

Oral bony outgrowths: Prevalence and genetic factor influence. Study of twins

Medicina, 2015
Objective: The aim of the study was to verify the influence of a genetic factor on the etiology of oral bony outgrowths and to determine the prevalence and type of oral bony outgrowths (tori and exostoses) among a group of Lithuanian twins. Materials and
Adomas Auškalnis, Olaf Bernhardt, Eglė Putnienė, Antanas Šidlauskas, Irena Andriuškevičiūtė, Nomeda Basevičienė   +5 more
doaj   +1 more source

Total knee arthroplasty in patients with multiple hereditary exostoses

Arthroplasty Today, 2018
We present a case report of a patient with severe valgus deformity of the right knee due to multiple hereditary exostoses (MHEs) treated with total knee arthroplasty (TKA). The surgical management of MHE affecting the knee encompasses exostoses resection,
Samuel A. Fernandez-Perez, MD, Julio A. Rodriguez, Jr., BS, David Beaton-Comulada, MD, Roberto G. Colon-Miranda, MD, Antonio H. Soler-Salas, MD, Antonio Otero-Lopez, MD   +5 more
doaj   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

Developmental Dynamics, EarlyView.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki, Rinna Kanai, Sayuri Tatsuta, Shinichi Kawaguchi, Masatsune Itoh, Shinsuke Ohba, Makoto Abe   +6 more
wiley   +1 more source