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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...
Autores principales: | Torrez, Timothy W, Marks, Elizabeth, Strom, Shane, Doyle, John Scott |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Orthopaedic Research Group
2021
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Materias: | |
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 |
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