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An unusual diagnosis for an usual test
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 number...
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| Pubblicato in: | Ital J Pediatr |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7285577/ https://ncbi.nlm.nih.gov/pubmed/32522262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-020-00846-z |
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