Results 21 to 30 of about 219 (121)

Post‐surgical infections: Prevalence associated with various periodontal surgical procedures

Journal of Periodontology, EarlyView.
Abstract Background This retrospective study aimed to assess the prevalence of postoperative infections after periodontal and implant surgical therapy and examined the treatment variables that may affect infection prevalence. Methods A retrospective review on patients who were surgically treated in the graduate periodontics clinic at the University of ...
Camille N. Banson, Archontia Palaiologou, Brian L. Mealey, Kerri Font, Charles A. Powell   +4 more
wiley   +1 more source

Long‐term stability of periodontal plastic surgery featuring traditional autogenous graft and coronally advanced flap alone

Periodontology 2000, EarlyView.
Abstract Background Coronally advanced flap (CAF), either alone or in combination with a connective tissue graft (CTG), represents one of the most extensively investigated surgical approaches for the treatment of gingival recessions, demonstrating high rates of mean root coverage (MRC) and complete root coverage (CRC). However, evidence regarding their
Giovanni Zucchelli, Ilham Mounssif, Claudio Mazzotti, Diego Bianchelli, Valentina Bentivogli, Matteo Marzadori, Matteo Sangiorgi, Alessandro Zucchelli, Monica Mele, Martina Stefanini   +9 more
wiley   +1 more source

Congenital multiple exostoses with congenital heart disease

Medical Journal of Dr. D.Y. Patil University, 2017
Multiple exostoses are a rare disorder. It is estimated to occur in 1; 50,000 pregnancies. It presents within the first decade of life and it has an autosomal mode of inheritance; though it has been associated with a spontaneous mutation in 10% of cases.
Ibrahim Aliyu, Teslim O Lawal
doaj   +1 more source

Surgical considerations based on oral and periodontal vascularization

Periodontology 2000, EarlyView.
Abstract Objectives To synthesize current evidence on vascular and anastomotic patterns, emphasizing their operative implications for optimizing flap perfusion, neovascularization, and wound healing in periodontal and implant surgery, while accounting for anatomical variability and collateral circulation. Materials and Methods A comprehensive review of
Arvin Shahbazi, Edward P. Allen, Sebastian Gschwindt, Kevin G. Murphy, Gábor Baksa, Anton Sculean   +5 more
wiley   +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

High‐Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient‐Reported Data

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 1989-1999, September 2026.
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George, Bamelak T. Duki, Zoe S. Katz, Aravind Viswanathan, Suzanne P. MacFarland, Evan R. Hathaway, Caitlin Monahan, John Morris, Kelly L. Trout, Shari M. Krantz, Arupa Ganguly, Jennifer M. Kalish   +11 more
wiley   +1 more source

Chronic Pain as an Early Diagnostic Clue in Hereditary Multiple Exostoses: Two Pediatric Cases Highlighting Diagnostic Delay

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Hereditary multiple exostoses (HME) is a rare autosomal dominant skeletal disorder characterized by the development of multiple osteochondromas adjacent to the growth plates. Although skeletal deformities and palpable masses are common findings, chronic pain may represent an early and underappreciated diagnostic clue, particularly in pediatric
Melissa Mariti Fraga, Valesca Oliveira Paes Tanaka, Luciana Tudech Salgueiro Pedro Paulo, Maria Carolina Santos, Carolina Costa Figueiredo, Nara Michelle de Araújo Evangelista, Vânia de Fátima Tonetto Fernandes, Guido de Paula Colares Neto   +7 more
wiley   +1 more source

Cervical osteoma in hereditary multiple exostoses

Journal of Pediatric Neurosciences, 2021
Osteoid osteoma is a benign bony pathology. It presents either as a solitary lesion or as multiple lesions with a genetic predisposition. Reported more often in teenagers with thrice more common incidence among boys than in girls, it has a predilection for long bones of lower limbs.
Chaturvedi, Jitender, Kumar, Niraj, Shakya, Jitendra, Sharma, Anil Kumar   +3 more
openaire   +2 more sources

Ankle Mortise Instability in Multiple Hereditary Exostoses

Foot & Ankle Orthopaedics, 2019
Category: Ankle, Ankle Arthritis, Pediatric Foot and Ankle Introduction/Purpose: Ankle valgus has been reported in 50% of patients with multiple hereditary exostoses (MHE) and, untreated, results in early arthrosis. Widening of the ankle mortise has also
M Pierce Ebaugh DO, Greg Grenier DO, Satbir Singh, Oussama Abousamra MD, Kevin Klingele MD   +4 more
doaj   +1 more source

Kyphoscoliosis as a skeletal malformation in a domestic corn snake (Pantherophis guttatus)

Veterinary Record Case Reports, Volume 14, Issue 3, August 2026.
Abstract Skeletal malformations in snakes represent an intriguing yet challenging aspect of veterinary medicine, as they can lead to significant impairment of patients’ mobility and therefore to poor quality of life. Reported skeletal malformations include proliferative osteoarthritis, osteoarthrosis, metabolic bone disease, Paget's disease or ...
Milena Tegelkamp, Eva Dervas, Katarzyna Walczak, Eva Maria Dutitre, Francesca Del Chicca   +4 more
wiley   +1 more source