This paper highlights a rare case of Osteogenesis imperfecta with description of clinical features, radiographic findings and its future prospects in the management.Saigal, AnjaliSamdani, DeepakSodhi, SPSPuri, NidhiArora, Gagandeep
Type IV is the most variable of the manifestations of osteogenesis imperfecta (Goldman, 1995: 4112). However, survival into adulthood is fairly common. Show moreView chapter Review article Topics in Bone and Bone Related Disorders Oral and Maxillofacial Surgery Clinics of North America Journal2007,...
Review of the literature with presentation of 29 cases Twelve families with 29 patients showing various patterns of osteogenesis imperfecta are described, along with the genetic, pathological, and clinical feat... Y Shoenfeld - 《American Journal of Diseases of Children》 被引量: 42发表: 1975年 ...
Professors Hamdy et al. deliver a comprehensive review of both modern osteogenesis imperfecta (OI) care and many developments put forth by their team and center over the years. The Montreal Center has been a giant in the field of OI care and research, and there are many pearls within the c...
Osteogenesis imperfecta (OI) is a rare heritable connective tissue disorder primarily characterised by skeletal deformity and fragility, and an array of secondary features. The purpose of this review was to capture and quantify the published evidence relating specifically to the clinical, humanistic, and...
Osteogenesis imperfecta (OI) describes a group of rare heritable disorders of connective tissue characterized by varying degrees of low bone mass and increased susceptibility to fractures. Most cases of OI are due to heritable defects in the synthesis or metabolism of type I collagen. The resulting...
Pain experiences of adults with Osteogenesis Imperfecta: An integrative reviewLobsteinbrittle boneknowledge synthesispain managementpain measurementpain perceptionThe Iconic Pain Assessment Tool (IPAT) is a novel web-based instrument for the self-report of pain quality, intensity and location in the form ...
Pathophysiology of respiratory failure in patients with osteogenesis imperfecta: a systematic review. Ann Med. 2021;53(1):1676–87. Article CAS PubMed PubMed Central Google Scholar Laurent GJ. Lung collagen: more than scaffolding. Thorax. 1986;41(6):418–28. Article CAS PubMed PubMed ...
The IMPACT survey: a mixed methods study to understand the experience of children, adolescents and adults with osteogenesis imperfecta and their caregivers ArticleOpen access21 March 2024 The psychosocial experience of individuals living with osteogenesis imperfecta: a mixed-methods systematic review ...
Osteogenesis imperfecta (OI), an inherited connective tissue disorder of remarkable clinical variability, is caused by a quantitative or qualitative defect in collagen synthesis and is characterised by bone fragility. The number of fractures and deformities, and the age at which they begin greatly infl...