Developmental motor impairment with lower limb spasticity most commonly corresponds to cerebral palsy of the spastic diplegia type. Here we describe a 4-year-old girl whose locomotor phenotype reflects early cortico-spinal lesion at the spinal level. This child has developmental spastic paraparesis secondary to D4-D8 cord compression. We analysed her gait using the ELITE optoelectronic system and compared it to that of six normal age-matched controls and six age-matched children with leucomalacic spastic diplegia. Gait characteristics of the patient included preservation of head orientation and arm swing similar to findings in normal controls and contrasting with children with spastic diplegia. She also had truncal instability and displayed lack of selectivity in lower limb movement as in spastic diplegia and in contrast with normal controls. This may reflect differences in locomotor control between developmental spasticity of cerebral and spinal origin. The latter might correspond to spinal palsy defined as abnormal movement and posture secondary to non-progressive pathological processes affecting the immature spinal cord.
%0 Journal Article
%1 Dan2004
%A Dan, Bernard
%A Bouillot, Ethel
%A Mewasingh, Leena D
%A Devalck, Christine
%A Bengoetxea, Ana
%A Christophe, Catherine
%A Ch?ron, Guy
%D 2004
%J Brain Dev
%K Arm; Cerebral Palsy; Child, Preschool; Diagnosis, Differential; Female; Gait; Gait Disorders, Neurologic; Head Movements; Humans; Infant; Infant, Newborn; Leg; Leukomalacia, Periventricular; Magnetic Resonance Imaging; Male; Mediastinal Neoplasms; Muscle Spasticity; Musculoskeletal Equilibrium; Paraplegia; Pyramidal Tracts; Reference Values; Spinal Cord Compression; Thoracic Vertebrae
%N 7
%P 463--468
%R 10.1016/j.braindev.2004.01.003
%T Gait control in spinal palsy.
%U http://dx.doi.org/10.1016/j.braindev.2004.01.003
%V 26
%X Developmental motor impairment with lower limb spasticity most commonly corresponds to cerebral palsy of the spastic diplegia type. Here we describe a 4-year-old girl whose locomotor phenotype reflects early cortico-spinal lesion at the spinal level. This child has developmental spastic paraparesis secondary to D4-D8 cord compression. We analysed her gait using the ELITE optoelectronic system and compared it to that of six normal age-matched controls and six age-matched children with leucomalacic spastic diplegia. Gait characteristics of the patient included preservation of head orientation and arm swing similar to findings in normal controls and contrasting with children with spastic diplegia. She also had truncal instability and displayed lack of selectivity in lower limb movement as in spastic diplegia and in contrast with normal controls. This may reflect differences in locomotor control between developmental spasticity of cerebral and spinal origin. The latter might correspond to spinal palsy defined as abnormal movement and posture secondary to non-progressive pathological processes affecting the immature spinal cord.
@article{Dan2004,
abstract = {Developmental motor impairment with lower limb spasticity most commonly corresponds to cerebral palsy of the spastic diplegia type. Here we describe a 4-year-old girl whose locomotor phenotype reflects early cortico-spinal lesion at the spinal level. This child has developmental spastic paraparesis secondary to D4-D8 cord compression. We analysed her gait using the ELITE optoelectronic system and compared it to that of six normal age-matched controls and six age-matched children with leucomalacic spastic diplegia. Gait characteristics of the patient included preservation of head orientation and arm swing similar to findings in normal controls and contrasting with children with spastic diplegia. She also had truncal instability and displayed lack of selectivity in lower limb movement as in spastic diplegia and in contrast with normal controls. This may reflect differences in locomotor control between developmental spasticity of cerebral and spinal origin. The latter might correspond to spinal palsy defined as abnormal movement and posture secondary to non-progressive pathological processes affecting the immature spinal cord.},
added-at = {2014-07-19T19:17:37.000+0200},
author = {Dan, Bernard and Bouillot, Ethel and Mewasingh, Leena D and Devalck, Christine and Bengoetxea, Ana and Christophe, Catherine and Ch?ron, Guy},
biburl = {https://www.bibsonomy.org/bibtex/2bff263eb8b2e5012ba2f52e4e499a272/ar0berts},
doi = {10.1016/j.braindev.2004.01.003},
groups = {public},
interhash = {d29573b22a9b6748e76a331439140d8b},
intrahash = {bff263eb8b2e5012ba2f52e4e499a272},
journal = {Brain Dev},
keywords = {Arm; Cerebral Palsy; Child, Preschool; Diagnosis, Differential; Female; Gait; Gait Disorders, Neurologic; Head Movements; Humans; Infant; Infant, Newborn; Leg; Leukomalacia, Periventricular; Magnetic Resonance Imaging; Male; Mediastinal Neoplasms; Muscle Spasticity; Musculoskeletal Equilibrium; Paraplegia; Pyramidal Tracts; Reference Values; Spinal Cord Compression; Thoracic Vertebrae},
month = Oct,
number = 7,
pages = {463--468},
pii = {S0387760404000233},
pmid = {15351083},
timestamp = {2014-07-19T19:17:37.000+0200},
title = {Gait control in spinal palsy.},
url = {http://dx.doi.org/10.1016/j.braindev.2004.01.003},
username = {ar0berts},
volume = 26,
year = 2004
}