Lifetime impact of achondroplasia: Current evidence and perspectives on the natural history

Achondroplasia, the most common form of disproportionate short stature, is caused by a variant in the fibroblast growth factor receptor 3 (FGFR3) gene. Advances in drug treatment for achondroplasia have underscored the need to better understand the natural history of this condition. This article pro...

Full description

Saved in:
Bibliographic Details
Published inBone (New York, N.Y.) Vol. 146; p. 115872
Main Authors Hoover-Fong, Julie, Cheung, Moira S., Fano, Virginia, Hagenas, Lars, Hecht, Jacqueline T., Ireland, Penny, Irving, Melita, Mohnike, Klaus, Offiah, Amaka C., Okenfuss, Ericka, Ozono, Keiichi, Raggio, Cathleen, Tofts, Louise, Kelly, Dominique, Shediac, Renée, Pan, Wayne, Savarirayan, Ravi
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.05.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Achondroplasia, the most common form of disproportionate short stature, is caused by a variant in the fibroblast growth factor receptor 3 (FGFR3) gene. Advances in drug treatment for achondroplasia have underscored the need to better understand the natural history of this condition. This article provides a critical review and discussion of the natural history of achondroplasia based on current literature evidence and the perspectives of clinicians with extensive knowledge and practical experience in managing individuals with this diagnosis. This review draws evidence from recent and ongoing longitudinal natural history studies, supplemented with relevant cross-sectional studies where longitudinal research is lacking, to summarize the current knowledge on the nature, incidence, chronology, and interrelationships of achondroplasia-related comorbidities across the lifespan. When possible, data related to adults are presented separately from data specific to children and adolescents. Gaps in knowledge regarding clinical care are identified and areas for future research are recommended and discussed.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:8756-3282
1873-2763
1873-2763
DOI:10.1016/j.bone.2021.115872