Fractures in Osteogenesis Imperfecta: Pathogenesis, Treatment, Rehabilitation and Prevention

Publication date

2022-02-16

Authors

Nijhuis, Wouter H.ORCID 0000-0001-6683-7549
Verhoef, M.ISNI 0000000390374657
van Bergen, Christiaan
Weinans, HarrieORCID 0000-0002-2275-6170ISNI 0000000393288658
Sakkers, RalphISNI 0000000393122439

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Document Type

Article

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Abstract

Fractures in patients with osteogenesis imperfecta (OI) are caused by a decreased strength of bone due to a decreased quality and quantity of bone matrix and architecture. Mutations in the collagen type 1 encoding genes cause the altered formation of collagen type I, one of the principal building blocks of bone tissue. Due to the complexity of the disease and the high variation of the clinical problems between patients, treatment for these patients should be individually tailored. In general, short immobilization periods with flexible casting material, use of intramedullary implants, and simultaneous deformity correction are preferred. Multidisciplinary care with a broad view of the support needed for the patient and his/her living environment is necessary for the optimal rehabilitation of these patients. Increasing bone strength with exercise, medication, and sometimes alignment surgery is generally indicated to prevent fractures.

Keywords

Brittle bone disease, Collagen, Fracture, Osteogenesis imperfecta, Rehabilitation, Surgery, Pediatrics, Perinatology, and Child Health

Citation

Nijhuis, W, Verhoef, M, van Bergen, C, Weinans, H & Sakkers, R 2022, 'Fractures in Osteogenesis Imperfecta : Pathogenesis, Treatment, Rehabilitation and Prevention', Children, vol. 9, no. 2, 268. https://doi.org/10.3390/children9020268