Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects

SUMMARY: Osteogenesis imperfecta (OI) is a genetic disease with an estimated prevalence of 1 in 13,500 and 1 in 9700. The classification into subtypes of OI is important for prognosis and management. In this study, we established a clinical severity prediction model depending on multiple features of...

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Detalles Bibliográficos
Autores principales: Yang, Lin, Liu, Bo, Dong, Xinran, Wu, Jing, Sun, Chengjun, Xi, Li, Cheng, Ruoqian, Wu, Bingbing, Wang, Huijun, Tong, Shiyuan, Wang, Dahui, Luo, Feihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106613/
https://www.ncbi.nlm.nih.gov/pubmed/35044492
http://dx.doi.org/10.1007/s00198-021-06263-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106613/
https://www.ncbi.nlm.nih.gov/pubmed/35044492
http://dx.doi.org/10.1007/s00198-021-06263-0

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