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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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| Publicat a: | Ital J Pediatr |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | 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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