The search result changed since you submitted your search request. Documents might be displayed in a different sort order.
  • search hit 5 of 50
Back to Result List

Gait Initiation in Children with Rett Syndrome

Please always quote using this URN: urn:nbn:de:bvb:20-opus-119789
  • Rett syndrome is an X-linked neurodevelopmental condition mainly characterized by loss of spoken language and a regression of purposeful hand use, with the development of distinctive hand stereotypies, and gait abnormalities. Gait initiation is the transition from quiet stance to steady-state condition of walking. The associated motor program seems to be centrally mediated and includes preparatory adjustments prior to any apparent voluntary movement of the lower limbs. Anticipatory postural adjustments contribute to postural stability and toRett syndrome is an X-linked neurodevelopmental condition mainly characterized by loss of spoken language and a regression of purposeful hand use, with the development of distinctive hand stereotypies, and gait abnormalities. Gait initiation is the transition from quiet stance to steady-state condition of walking. The associated motor program seems to be centrally mediated and includes preparatory adjustments prior to any apparent voluntary movement of the lower limbs. Anticipatory postural adjustments contribute to postural stability and to create the propulsive forces necessary to reach steady-state gait at a predefined velocity and may be indicative of the effectiveness of the feedforward control of gait. In this study, we examined anticipatory postural adjustments associated with gait initiation in eleven girls with Rett syndrome and ten healthy subjects. Muscle activity (tibialis anterior and soleus muscles), ground reaction forces and body kinematic were recorded. Children with Rett syndrome showed a distinctive impairment in temporal organization of all phases of the anticipatory postural adjustments. The lack of appropriate temporal scaling resulted in a diminished impulse to move forward, documented by an impairment in several parameters describing the efficiency of gait start: length and velocity of the first step, magnitude and orientation of centre of pressure-centre of mass vector at the instant of (swing-)toe off. These findings were related to an abnormal muscular activation pattern mainly characterized by a disruption of the synergistic activity of antagonistic pairs of postural muscles. This study showed that girls with Rett syndrome lack accurate tuning of feedforward control of gait.show moreshow less

Download full text files

Export metadata

Additional Services

Share in Twitter Search Google Scholar Statistics
Metadaten
Author: Ioannis Ugo Isaias, Mariangela Dipaola, Marlies Michi, Alberto Marzegan, Jens Volkmann, Mariana L. Rodocanachi Roidi, Carlo Albino Frigo, Paolo Cavallari
URN:urn:nbn:de:bvb:20-opus-119789
Document Type:Journal article
Faculties:Medizinische Fakultät / Neurologische Klinik und Poliklinik
Language:English
Parent Title (English):PLoS ONE
ISSN:1932-6203
Year of Completion:2014
Volume:9
Issue:4
Pagenumber:e92736
Source:PLoS ONE 9(4): e92736. doi:10.1371/ journal.pone.0092736
DOI:https://doi.org/10.1371/journal.pone.0092736
Pubmed Id:https://pubmed.ncbi.nlm.nih.gov/24743294
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 618 Gynäkologie, Geburtsmedizin, Pädiatrie, Geriatrie
Tag:ankles  ; biological locomotion; children; kinematics; rett; soleus muscles; syndrome; velocity; walking
Release Date:2015/11/13
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung