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Arthroscopic Anterior Cruciate Ligament Reconstruction in a 17-Year-Old Female Athlete with Multiple Hereditary Exostoses Using a Peroneus Longus Autograft: A Rare Case Report [PDF]

Journal of Orthopaedic Case Reports
Introduction: Hereditary multiple exostoses, also known as multiple osteochondromas, is a rare genetic disorder marked by the formation of osteocartilaginous outgrowths predominantly near the metaphysis of long bones.
Sanjay Singh Chauhan, Harshita Udiwal, Narendra Singh Butola   +2 more
doaj   +2 more sources

Hereditary multiple osteochondromas in a child: a case report and discussion of postoperative complication management [PDF]

Frontiers in Surgery
BackgroundThe pathogenesis of hereditary multiple exostoses is mainly related to genetic variants and often requires surgical resection when it causes clinical symptoms.
Haiting Jia, Yuting Wang, Tao Liu
doaj   +2 more sources

Management of Lower Extremity Deformity in Children with Hereditary Multiple Exostoses [PDF]

Journal of the Pediatric Orthopaedic Society of North America
Hereditary multiple exostoses (HME) is a rare genetic disorder characterized by multiple benign, cartilage-capped bony tumors, most often found at the juxta-epiphyseal regions of long bones.
Matthew J. Whalen, MS, Harold J.P. van Bosse, MD   +1 more
doaj   +2 more sources

Hereditary Multiple Exostoses: Current Insights

Orthopedic Research and Reviews, 2019
Antonio D’Arienzo, Lorenzo Andreani, Federico Sacchetti, Simone Colangeli, Rodolfo Capanna Department of Translational Research on New Surgical and Medical Technologies, University of Pisa, Pisa, ItalyCorrespondence: Federico SacchettiDepartment of
D'Arienzo A, Andreani L, Sacchetti F, Colangeli S, Capanna R   +4 more
doaj   +4 more sources

Malignancy Ratio in Pediatric Patients with Hereditary Multiple Exostoses: True Association or Reporting Bias? [PDF]

Pediatric Reports
Background: Hereditary Multiple Exostoses (HME) is a rare autosomal dominant skeletal disorder resulting from loss-of-function variants in the EXT1, EXT2, or EXT3 genes. While malignant transformation into chondrosarcoma is well documented, the incidence
Francesco Fabrizio Comisi, Andrea Maria Comisi, Elena Esposito, Salvatore Savasta   +3 more
doaj   +2 more sources

Costal chondrosarcoma in a woman with hereditary multiple exostoses - a case report [PDF]

Frontiers in Oncology
In this report, we present a case of a 32-year-old female previously diagnosed with hereditary multiple exostoses(HME) who was incidentally found to have an asymptomatic anterior mediastinal mass during a routine examination.
Ze Yang, Kaiqiang Wang, Jiangtao Pu
doaj   +2 more sources

Hereditary multiple exostoses: an educational review [PDF]

Insights into Imaging
Hereditary multiple exostoses (HME), an autosomal dominant disorder with an incidence of 1:50,000 to 1:100,000, is characterised by the formation of multiple osteochondromas arising from the metaphyses of long and flat bones.
Alvaro Rueda-de-Eusebio, Sara Gomez-Pena, María José Moreno-Casado, Gloria Marquina, Juan Arrazola, Ana María Crespo-Rodríguez   +5 more
doaj   +2 more sources

Hereditary multiple exostoses

Ankara Üniversitesi Tıp Fakültesi Mecmuası, 2006
Şenay Savaş Erdeve, Yıldız Dallar, Sinan Aslan   +2 more
doaj   +4 more sources

Hereditary multiple exostoses

Medical Journal of Dr. D.Y. Patil University, 2017
Hasan Ekim, Meral Ekim
doaj   +3 more sources

A Family with Hereditary Multiple Exostoses [PDF]

Eurasian Journal of Family Medicine, 2021
Hereditary multiple exostoses is a rare autosomal dominant genetic disorder characterized by multiple exostoses (osteochondromas), mostly diagnosed in childhood.
Tahir Ismailoglu
doaj   +1 more source