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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
PMID: 25218933
Full text
Article (Published version) (838 Kb) - document accessible for UNIGE members only 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

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Deposited on : 2015-03-04

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