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Atypical femur fractures: a distinctive tract of adult hypophosphatasia
Hypophosphatasia (HPP) is a congenital, rare and heterogeneous bone disorder, characterized by a deficit of calcified tissue mineralization, leading to skeletal deformities and osteomalacia in adults, rickets in infants and children, and fragility fractures and premature loss of dentition in childre...
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| Publicado no: | Clin Cases Miner Bone Metab |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
CIC Edizioni Internazionali
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5762223/ https://ncbi.nlm.nih.gov/pubmed/29354161 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/ccmbm/2017.14.3.324 |
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