Gait evolution in a family with hereditary spastic paraplegia

Armand, Stéphane; Turcot, Katia; Bonnefoy-Mazure, Alice; Lascombes, Pierre François Marie; De Coulon, Geraldo

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Title		Gait evolution in a family with hereditary spastic paraplegia
Authors		Armand, Stéphane Turcot, Katia Bonnefoy-Mazure, Alice Lascombes, Pierre François Marie De Coulon, Geraldo
Published in		European Journal of Paediatric Neurology. 2015, vol. 19, no. 1, p. 87-92
Abstract		The degree of disability in patients with hereditary spastic paraplegia has been reported variable even in members of the same family (same gene mutation). Moreover, it has been established that patients with hereditary spastic paraplegia should be treated differently from cerebral palsy patients due to the progressive nature of this disease. However, the gait evolution of hereditary spastic paraplegia showing onset symptoms at an early age has been described as stable. Therefore, this study aims to evaluate the walking ability and the influence of treatments on gait evolution in a family with hereditary spastic paraplegia.
Identifiers		DOI: 10.1016/j.ejpn.2014.08.001 PMID: 25218933
Full text		Article (Published version) (838 Kb) - Limited access to UNIGE
Structures		Faculté de médecine / Section de médecine clinique / Département de chirurgie Faculté de médecine / Section de médecine clinique / Département de pédiatrie
Research groups		Groupe Lascombes Pierre (orthopédie pédiatrique) (917) Laboratoire de cinésiologie (943)
Citation (ISO format)		ARMAND, Stéphane et al. Gait evolution in a family with hereditary spastic paraplegia. In: European Journal of Paediatric Neurology, 2015, vol. 19, n° 1, p. 87-92. https://archive-ouverte.unige.ch/unige:47572