AB107. Study of functional independence of patients with osteogenesis imperfecta

BACKGROUND: Osteogenesis imperfecta (OI) is a genetic bone disorder characterized by fragile bones that break easily. It is a complicated, variable and rare disorder. Its major feature is a fragile skeleton, but many other body systems are also affected. OI is caused by a mutation in a gene that aff...

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Vydáno v:Ann Transl Med
Hlavní autoři: Nguyen, Thu Ha, Thuy, Linh Tran Thi, Thi, Xuan Bui, Thi, Huong Bui, Do Thi, Hoa, Thanh, Hoa Nguyen Thi, Do Thi, Mo, Thu, Ha Nguyen
Médium: Artigo
Jazyk:Inglês
Vydáno: AME Publishing Company 2017
Témata:
Birth Defects, Dysmorphology, Skeletal Dysplasia, Craniofacial Anomalies
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641763/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s107
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