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Gait Initiation in Children with Rett Syndrome

Zitieren Sie bitte immer diese 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.zeige mehrzeige weniger

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Autor(en): 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
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Neurologische Klinik und Poliklinik
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):PLoS ONE
ISSN:1932-6203
Erscheinungsjahr:2014
Band / Jahrgang:9
Heft / Ausgabe:4
Seitenangabe:e92736
Originalveröffentlichung / Quelle: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
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 618 Gynäkologie, Geburtsmedizin, Pädiatrie, Geriatrie
Freie Schlagwort(e):ankles  ; biological locomotion; children; kinematics; rett; soleus muscles; syndrome; velocity; walking
Datum der Freischaltung:13.11.2015
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung