Osteogenesis imperfecta

Neonatal Netw. 2004 Mar-Apr;23(2):7-14. doi: 10.1891/0730-0832.23.2.7.

Abstract

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.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Continuity of Patient Care / organization & administration
  • Female
  • Fetal Diseases / classification
  • Fetal Diseases / diagnosis
  • Fetal Diseases / nursing
  • Humans
  • Infant Care / methods
  • Infant, Newborn
  • Male
  • Neonatal Nursing / methods*
  • Osteogenesis Imperfecta / classification
  • Osteogenesis Imperfecta / diagnosis*
  • Osteogenesis Imperfecta / nursing*
  • Patient Discharge
  • Pregnancy
  • Prenatal Diagnosis / methods
  • Prenatal Diagnosis / nursing
  • Professional-Family Relations