Journal article
Quantitative measures of motor development in Angelman syndrome
- Abstract:
- Angelman Syndrome is a rare neurodevelopmental disorder characterized by developmental delay, lack of speech, seizures, intellectual disability, characteristic behavior, and movement disorders. Clinical gait analysis provides the opportunity for movement quantification to investigate an observed maladaptive change in gait pattern and offers an objective outcome of change. Pressure-sensor-based technology, inertial and activity monitoring, and instrumented gait analysis (IGA) were employed to define motor abnormalities in Angelman syndrome. Temporal-spatial gait parameters of persons with Angelman Syndrome (pwAS) show deficiencies in gait performance through walking speed, step length, step width, and walk ratio. pwAS walk with reduced step lengths, increased step width, and greater variability. Three-dimensional motion kinematics showed increased anterior pelvic tilt, hip flexion, and knee flexion. PwAS have a walk ratio more than two standard deviations below controls. Dynamic electromyography showed prolonged activation of knee extensors, which was associated with a decreased range of motion and the presence of hip flexion contractures. Use of multiple gait tracking modalities revealed that pwAS exhibit a change in gait pattern to a flexed knee gait pattern. Cross-sectional studies of individuals with AS show a regression toward this maladaptive gait pattern over development in pwAS ages 4-11. PwAS unexpectedly did not have spasticity associated with change in gait pattern. Multiple quantitative measures of motor patterning may offer early biomarkers of gait decline consistent with critical periods of intervention, insight into appropriate management strategies, objective primary outcomes, and early indicators of adverse events.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Accepted manuscript, pdf, 864.0KB, Terms of use)
-
- Publisher copy:
- 10.1002/ajmg.a.63192
Authors
+ Eunice Kennedy Shriver National Institute of Child Health and Human Development
More from this funder
- Funder identifier:
- https://ror.org/04byxyr05
- Publisher:
- Wiley
- Journal:
- American Journal of Medical Genetics - Part A More from this journal
- Volume:
- 191
- Issue:
- 7
- Pages:
- 1711-1721
- Place of publication:
- United States
- Publication date:
- 2023-04-05
- Acceptance date:
- 2023-03-10
- DOI:
- EISSN:
-
1552-4833
- ISSN:
-
1552-4825
- Pmid:
-
37019838
- Language:
-
English
- Keywords:
- Pubs id:
-
1337152
- UUID:
-
uuid_506d3ad4-7765-49d2-b87b-7da3e25a01fa
- Local pid:
-
pubs:1337152
- Source identifiers:
-
W4362602816
- Deposit date:
-
2025-12-11
- ARK identifier:
Terms of use
- Copyright holder:
- Wiley Periodicals LLC.
- Copyright date:
- 2023
- Rights statement:
- © 2023 Wiley Periodicals LLC.
- Notes:
- This is the accepted manuscript version of the article. The final version is available online from Wiley at https://dx.doi.org/10.1002/ajmg.a.63192
If you are the owner of this record, you can report an update to it here: Report update to this record