A Case Report of Trevor’s Disease in a Pediatric Patient with Hereditary Multiple Exostoses Disease

INTRODUCTION: Hereditary multiple exostoses (HME) disease is hallmarked by cartilaginous osteochondromas secondary to an autosomal dominant mutation within the exostosin gene family. These outgrowths predominantly occur around the long bone physis. An associated disease is dysplasia epiphysealis hem...

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Detalles Bibliográficos
Autores principales: Torrez, Timothy W, Marks, Elizabeth, Strom, Shane, Doyle, John Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930384/
https://www.ncbi.nlm.nih.gov/pubmed/35415146
http://dx.doi.org/10.13107/jocr.2021.v11.i12.2558

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930384/
https://www.ncbi.nlm.nih.gov/pubmed/35415146
http://dx.doi.org/10.13107/jocr.2021.v11.i12.2558

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