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1. Introduction Multiple Hereditary Exostosis (MHE) is a rare orthopedic disorder which is responsible for abnormal cartilage and bone growth [1,2]. The incidence is between one and two cases/100,000 habitants/year and it has a clear male predilection [3]. Basic research has identified several genetical abnormalities determining the disease, such as a mutation of the EXT1 gene on chromosome 8 or EXT2 gene on chromosome 11 [1,2,3].
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