{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,8,28]],"date-time":"2023-08-28T12:19:59Z","timestamp":1693225199588},"reference-count":27,"publisher":"Springer Publishing Company","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neonatal Network"],"published-print":{"date-parts":[[2004,3]]},"abstract":"<jats:p>Osteogenesis imperfecta (OI) is a rare congenital disorder of collagen production that results in brittle bones and affects other body systems containing collagen. This article reviews the current body of knowledge about OI and the management of infants with the disorder. Relieving pain, reducing the incidence of new fractures, establishing adequate follow-up, and connecting parents with community resources are the goals of management during the neonatal period. A case study illustrates management and the discharge process.<\/jats:p>","DOI":"10.1891\/0730-0832.23.2.7","type":"journal-article","created":{"date-parts":[[2011,11,16]],"date-time":"2011-11-16T09:55:04Z","timestamp":1321437304000},"page":"7-14","source":"Crossref","is-referenced-by-count":7,"title":["Osteogenesis Imperfecta"],"prefix":"10.1891","volume":"23","author":[{"given":"Kathryn","family":"McLean","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"793","published-online":{"date-parts":[[2004,3,1]]},"reference":[{"key":"1","unstructured":"Osteogenesis Imperfecta Foundation. 2001. Caring for infants & children with osteogenesis imperfecta: A publication of the Osteogenesis Imperfecta Foundation. Retrieved October 14, 2001, from <a target=\"_blank\" href='http:\/\/oif.convio.com\/site\/PageServer?pagename=InfChild'>http:\/\/oif.convio.com\/site\/PageServer? pagename= InfChild<\/a>"},{"issue":"1","key":"2","doi-asserted-by":"crossref","first-page":"7","DOI":"10.3109\/07853890109002055","article-title":"Collagens and collagenrelated diseases.","volume":"33","author":"J Myllyharju","year":"2001","journal-title":"Annals of Medicine"},{"issue":"11","key":"3","doi-asserted-by":"crossref","first-page":"876","DOI":"10.1002\/1097-0223(200011)20:11<876::AID-PD936>3.0.CO;2-X","article-title":"Prenatal diagnosis of a novel COL1A1 mutation in osteogenesis imperfecta Type I carried through full term pregnancy.","volume":"20","author":"L Ries","year":"2000","journal-title":"P renatal Diagnosis"},{"issue":"9","key":"4","doi-asserted-by":"crossref","first-page":"746","DOI":"10.1001\/jama.1997.03540330068037","article-title":"Osteogenesis imperfecta: Rehabilitation and prospects for gene therapy.","volume":"277","author":"J Marini","year":"1997","journal-title":"JAMA"},{"issue":"2","key":"5","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1136\/jmg.16.2.101","article-title":"Genetic heterogeneity in osteogenesis imperfecta.","volume":"16","author":"D Sillence","year":"1979","journal-title":"Journal of Medical Genetics"},{"issue":"4","key":"6","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1136\/jmg.32.4.284","article-title":"Perinatal lethal osteogenesis imperfecta.","volume":"32","author":"W Cole","year":"1995","journal-title":"Journal of Medical Genetics"},{"issue":"5","key":"7","first-page":"558","article-title":"Osteogenesis imperfecta: A review of basic science and diagnosis.","volume":"21","author":"C Minch","year":"1998","journal-title":"Orthopedics"},{"key":"8","unstructured":"Jones K. 1996. <i>Smith's Recognizable Patterns of Human Malformation<\/i>, 5th ed., Philadelphia: WB Saunders, 486\u2013489."},{"issue":"401","key":"9","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1097\/00003086-200208000-00003","article-title":"Advances in osteogenesis imperfecta.","volume":"August","author":"W. Cole","year":"2002","journal-title":"Clinics in O rthopedics"},{"issue":"1","key":"10","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1359\/jbmr.2002.17.1.30","article-title":"Osteogenesis imperfecta Type VI: A form of brittle bone disease with a mineralization defect.","volume":"17","author":"F Glorieux","year":"2002","journal-title":"Journal of Bone and Mineralization Reserves"},{"issue":"1","key":"11","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1016\/S8756-3282(02)00808-6","article-title":"Osteogenesis imperfecta Type VII maps to the short arm of chromosome 3.","volume":"31","author":"M Labuda","year":"2002","journal-title":"Bone"},{"issue":"1","key":"12","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1016\/S8756-3282(02)00790-1","article-title":"Osteogenesis imperfecta Type VII: An autosomal recessive form of brittle bone disease.","volume":"31","author":"L Wa rd","year":"2002","journal-title":"Bone"},{"key":"13","unstructured":"Osteogenesis Imperfecta Foundation. 2003. Osteogenesis Imperfecta: A Guide for Nurses. Retrieved November 12, 2003, from <a target=\"_blank\" href='http:\/\/www.oif.org\/site\/DocServer\/Web_Version.pdf?docID=181'>http:\/\/www.oif.org\/site\/DocServer\/Web_Version.pdf?docID= 181<\/a>"},{"issue":"1","key":"14","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1016\/S0029-7844(00)01100-5","article-title":"Osteogenesis imperfecta: Mode of delivery and neonatal outcome.","volume":"97","author":"R Cubert","year":"2001","journal-title":"Obstetrics and Gynecology"},{"issue":"2","key":"15","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1097\/01241398-200003000-00027","article-title":"Intramedullary rodding in osteogenesis imperfecta.","volume":"20","author":"K Mulpuri","year":"2000","journal-title":"Journal of Pediatric Orthopaedics"},{"issue":"1","key":"16","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1097\/00002508-199603000-00004","article-title":"Premature infant pain profile: Development and initial validation.","volume":"12","author":"B Stevens","year":"1996","journal-title":"Clinical Journal of Pain"},{"issue":"9","key":"17","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1097\/00000446-200209000-00065","article-title":"Pain assessment in infants and young children: Premature infant pain profile.","volume":"102","author":"C. 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Open-label study in seven patients.","volume":"69","author":"F Giraud","year":"2002","journal-title":"Joint Bone Spine"},{"issue":"supplement 6","key":"23","first-page":"1491","article-title":"The use of bisphosphonates in children with osteogenesis imperfecta.","volume":"14","author":"F. 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