Results 21 to 30 of about 1,979 (168)

Osteochondroma of Upper Dorsal Spine Causing Spastic Paraparesis in Hereditary Multiple Exostosis: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2015
Osteochondroma of the spine is rare. It may present in solitary or multiple form (hereditary multiple exostoses). Herein, we report a case of an 18-year-old male who was diagnosed with thoracic osteochondroma, originating from the D4 vertebra with ...
Gaurav Kumar Upadhyaya, Vijay Kumar Jain, Rajendra Kumar Arya, Skand Sinha, Ananta Kumar Naik   +4 more
doaj   +1 more source

Reconstruction of the Hip in Multiple Hereditary Exostoses

Children, 2021
The hip joint involvement in multiple hereditary exostoses (MHE) occurs in 30–90%, causing pain and limitation of motion by femoroacetabular impingement, coxa valga, acetabular dysplasia, hip joint subluxation, and osteoarthritis.
Dong Hoon Lee, Dror Paley
doaj   +1 more source

Hereditary multiple exostoses with a giant osteochondroma degenerated into chondrosarcoma

Radiology Case Reports
We present a case of hereditary multiple exostoses with malignant transformation to chondrosarcoma in a woman complaining of enlargement and pain in the right thigh.
Federica Masino, MD, Manuela Montatore, MD, Rossella Carpentiere, MD, Marina Balbino, MD, Rossella Gifuni, MD, Giacomo Fascia, MD, Giuseppe Guglielmi, MD   +6 more
doaj   +1 more source

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

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

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

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

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