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Gait initiation in children with Rett syndrome
Ioannis Ugo Isaias1, Mariangela Dipaola2, Marlies Michi3
1Department of Neurology, University Hospital Würzburg, Würzburg, Germany; Department of Pathophysiology and Transplantation, LAMB Pierfranco & Luisa Mariani, University of Milan, Milan, Italy.
Plos One
|April 19, 2014
Summary
Girls with Rett syndrome exhibit impaired gait initiation due to disrupted anticipatory postural adjustments. This neurodevelopmental condition affects motor control, impacting the feedforward control of gait.
Area of Science:
- Neuroscience
- Developmental Biology
- Biophysics
Background:
- Rett syndrome is an X-linked neurodevelopmental disorder.
- Gait abnormalities are a key characteristic of Rett syndrome.
- Gait initiation involves complex, centrally mediated motor programs.
Purpose of the Study:
- To investigate anticipatory postural adjustments during gait initiation in girls with Rett syndrome.
- To compare motor control strategies between individuals with Rett syndrome and healthy controls.
- To identify specific impairments in gait initiation related to Rett syndrome.
Main Methods:
- Electromyography of tibialis anterior and soleus muscles.
- Measurement of ground reaction forces.
- Analysis of body kinematics during gait initiation.
Main Results:
- Girls with Rett syndrome demonstrated impaired temporal organization of anticipatory postural adjustments.
- Deficits in temporal scaling led to reduced forward propulsion and altered first step parameters.
- Abnormal muscle activation patterns, including disrupted synergistic activity, were observed.
Conclusions:
- Girls with Rett syndrome exhibit significant impairments in the feedforward control of gait initiation.
- The findings highlight a lack of accurate tuning in motor control mechanisms.
- This study provides insights into the motor deficits associated with Rett syndrome.

