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Review
. 2017 Apr 4:10:145-155.
doi: 10.2147/JMDH.S113483. eCollection 2017.

Managing the patient with osteogenesis imperfecta: a multidisciplinary approach

Affiliations
Review

Managing the patient with osteogenesis imperfecta: a multidisciplinary approach

Caroline Marr et al. J Multidiscip Healthc. .

Abstract

Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized by low bone density. The type and severity of OI are variable. The primary manifestations are fractures, bone deformity, and bone pain, resulting in reduced mobility and function to complete everyday tasks. OI affects not only the physical but also the social and emotional well-being of children, young people, and their families. As such, medical, surgical, and allied health professionals' assessments all play a role in the management of these children. The multidisciplinary approach to the treatment of children and young people living with OI seeks to provide well-coordinated, comprehensive assessments, and interventions that place the child and family at the very center of their care. The coordinated efforts of a multidisciplinary team can support children with OI to fulfill their potential, maximizing function, independence, and well-being.

Keywords: bisphosphonates; nursing; occupational therapy; pediatrics; physical therapy; psychology.

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Conflict of interest statement

Disclosure The authors report no conflicts of interest in this work.

References

    1. Forlino A, Cabral WA, Barnes AM, Marini JC. New perspectives on osteogenesis imperfecta. Nat Rev Endocrinol. 2011;7(9):540–557. - PMC - PubMed
    1. Dogba MJ, Rauch F, Tre G, Glorieux FH, Bedos C. Shaping and managing the course of a child’s disease: parental experiences with osteogenesis imperfecta. Disabil Health J. 2014;7(3):343–349. - PubMed
    1. Marini JC, Reich A, Smith SM. Osteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formation. Curr Opin Pediatr. 2014;26(4):500–507. - PMC - PubMed
    1. Shapiro JR, Byers PH, Glorieux FH, Sponseller P. Osteogenesis Imperfecta: A Translational Approach to Brittle Bone Disease. Cambridge, MA: Academic Press; 2013.
    1. Shaker JL, Albert C, Fritz J, Harris G. Recent developments in osteogenesis imperfecta. F1000Res. 2015;4(F1000 Faculty Rev):681. - PMC - PubMed