Functional Change in a Child With Achondroplasia Following 12 Months Treatment With Vosoritide—A Case Report

Achondroplasia is the most common form of skeletal dysplasia. Over the last 24 months, a new treatment (vosoritide) is now available to promote endochondral growth through a daily injection. While research has identified increased annualized growth velocity in children with achondroplasia receiving vosoritide injections, there is currently little information on functional change and independence in self-care following this treatment. Here, we present a 5-year-old boy with achondroplasia who received vosoritide injections for 12 months. His functional performance was measured using the Functional Independence Measure for Children (WeeFIM). He was found to have a slightly higher level of independence when compared to age-matched peers with achondroplasia, and his rate of improvement in independence skills was twice that recorded in a previous study monitoring independence in children with achondroplasia following 12 months on vosoritide. When compared with WeeFIM normative data from average-statured children across the 12 months from 4 to 5 years, our child demonstrated almost three times the change for total WeeFIM and Self-Care domain scores and nine times the change across the Mobility domain scores, indicating a rapid increase in independence development. Our findings suggest that vosoritide may support the improvement of functional independence in children with achondroplasia receiving vosoritide to increase bone growth.

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Publication Details

Journal
American Journal of Medical Genetics Part A
Published
2025-03-18
DOI
https://doi.org/10.1002/ajmg.a.64054
Citations
3
Primary Topic
Connective tissue disorders research
Type
article
Field-Weighted Citation Impact
5.45
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article

Functional Change in a Child With Achondroplasia Following 12 Months Treatment With Vosoritide—A Case Report

Penelope J. Ireland, Craig F. Munns, E. Pendlebury, Theresa L. Carroll et al.
3 citations
American Journal of Medical Genetics Part A
Connective tissue disorders research
5.45
article

Functional Change in a Child With Achondroplasia Following 12 Months Treatment With Vosoritide—A Case Report

Penelope J. Ireland, Craig F. Munns, E. Pendlebury, Theresa L. Carroll, Eleanor Weston
article en
3 citations

Abstract

Achondroplasia is the most common form of skeletal dysplasia. Over the last 24 months, a new treatment (vosoritide) is now available to promote endochondral growth through a daily injection. While research has identified increased annualized growth velocity in children with achondroplasia receiving vosoritide injections, there is currently little information on functional change and independence in self-care following this treatment. Here, we present a 5-year-old boy with achondroplasia who received vosoritide injections for 12 months. His functional performance was measured using the Functional Independence Measure for Children (WeeFIM). He was found to have a slightly higher level of independence when compared to age-matched peers with achondroplasia, and his rate of improvement in independence skills was twice that recorded in a previous study monitoring independence in children with achondroplasia following 12 months on vosoritide. When compared with WeeFIM normative data from average-statured children across the 12 months from 4 to 5 years, our child demonstrated almost three times the change for total WeeFIM and Self-Care domain scores and nine times the change across the Mobility domain scores, indicating a rapid increase in independence development. Our findings suggest that vosoritide may support the improvement of functional independence in children with achondroplasia receiving vosoritide to increase bone growth.

American Journal of Medical Genetics Part AVol. 197(7)
The University of Queensland (AU), Children's Health Queensland Hospital and Health Service (AU)
Openalex Percentile: Top 5%
Connective tissue disorders research
5.45
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