An unusual diagnosis for an usual test
Abstract Background Hereditary multiple osteochondromas (HMO) is a genetic condition characterized by the presence of multiple osteochondromas, usually at the lateral side of the most active growth plate of a long bone. These lesions may persist, be asymptomatic during childhood, and may increase in...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2020-06-01
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Series: | Italian Journal of Pediatrics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13052-020-00846-z |