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Osteopetrosis and Chiari type I malformation: a rare association
Osteopetrosis (OP) is hereditary X-linked, autosomal recessive (ARO), or autosomal dominant (ADO) skeletal disease. ARO has two subtypes, which are infantile malignant and intermediate type. ARO and X-linked OP have poor clinical outcome. ADO is called adult benign type because of the normal life ex...
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| Pubblicato in: | J Surg Case Rep |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4620537/ https://ncbi.nlm.nih.gov/pubmed/26503583 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jscr/rjv084 |
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