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The genetic implication of scoliosis in osteogenesis imperfecta: a review
Osteogenesis imperfecta (OI) is a kind of heritable connective tissue disorder, including blue sclerae, hearing loss, skeletal dysplasia causing bone fragility and deformities. It is typically caused by collagen related gene mutations, which could lead to bone formation abnormalities. Scoliosis is o...
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| Publicado no: | J Spine Surg |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5760423/ https://ncbi.nlm.nih.gov/pubmed/29354746 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/jss.2017.10.01 |
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