Clinical manifestations of osteogenesis imperfecta in adulthood: An integrative review of quantitative studies and case reports. Issue 4 (24th February 2020)
- Record Type:
- Journal Article
- Title:
- Clinical manifestations of osteogenesis imperfecta in adulthood: An integrative review of quantitative studies and case reports. Issue 4 (24th February 2020)
- Main Title:
- Clinical manifestations of osteogenesis imperfecta in adulthood: An integrative review of quantitative studies and case reports
- Authors:
- Chougui, Khadidja
Addab, Sofia
Palomo, Telma
Morin, Suzanne N.
Veilleux, Louis‐Nicolas
Bernstein, Mitchell
Thorstad, Kelly
Hamdy, Reggie
Tsimicalis, Argerie - Abstract:
- Abstract: Osteogenesis imperfecta (OI) is a rare genetic disorder of the bones caused by a mutation in Type I collagen genes. As adults with OI are aging, medical concerns secondary to OI may arise. This integrative review sought to review, appraise, and synthesize the clinical manifestations faced by adults with OI. Four electronic bibliographic databases were searched. Published quantitative, qualitative, and mixed‐methods studies, as well as case reports from 2000 to March 2019, addressing a clinical manifestation in adulthood, were reviewed. Eligible studies and case reports were subsequently appraised using the Mixed Methods Appraisal Tool and Case Report Checklist, respectively. Twenty quantitative studies and 88 case reports were included for review regardless of the varying methodological quality score. These studies collectively included 2, 510 adults with different OI types. Several clinical manifestations were studied, and included: hearing loss, cardiac diseases, pregnancy complications, cerebrovascular manifestations, musculoskeletal manifestations, respiratory manifestations, vision impairment, and other clinical manifestations. Increased awareness may optimize prevention, treatment, and follow‐up. Opportunities to enhance the methodological quality of research including better design and methodology, multisite collaborations, and larger and diverse sampling will optimize the generalizability and transferability of findings.
- Is Part Of:
- American journal of medical genetics. Volume 182:Issue 4(2020)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 182:Issue 4(2020)
- Issue Display:
- Volume 182, Issue 4 (2020)
- Year:
- 2020
- Volume:
- 182
- Issue:
- 4
- Issue Sort Value:
- 2020-0182-0004-0000
- Page Start:
- 842
- Page End:
- 865
- Publication Date:
- 2020-02-24
- Subjects:
- adults -- brittle bones disease -- clinical manifestations -- integrative review -- knowledge synthesis -- osteogenesis imperfecta
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.61497 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13171.xml