Tremor as the first neurological manifestation of Sneddon's syndrome.
Identifieur interne : 000F58 ( Ncbi/Curation ); précédent : 000F57; suivant : 000F59Tremor as the first neurological manifestation of Sneddon's syndrome.
Auteurs : A Martins Da Silva [Portugal] ; N. Rocha ; M. Pinto ; V. Alves ; F. Farinha ; A P Correia ; T. Coelho ; M. MagalhãesSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2005.
English descriptors
- KwdEn :
- Anticonvulsants (therapeutic use), Brain (pathology), Clonazepam (therapeutic use), Electroencephalography (methods), Female, Humans, Lateral Ventricles (pathology), Magnetic Resonance Imaging (methods), Middle Aged, Neurologic Examination (methods), Phenobarbital (therapeutic use), Sneddon Syndrome (drug therapy), Sneddon Syndrome (pathology), Sneddon Syndrome (physiopathology), Tremor (drug therapy), Tremor (etiology).
- MESH :
- chemical , therapeutic use : Anticonvulsants, Clonazepam, Phenobarbital.
- drug therapy : Sneddon Syndrome, Tremor.
- etiology : Tremor.
- methods : Electroencephalography, Magnetic Resonance Imaging, Neurologic Examination.
- pathology : Brain, Lateral Ventricles, Sneddon Syndrome.
- physiopathology : Sneddon Syndrome.
- Female, Humans, Middle Aged.
Abstract
We report on a 54-year-old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2-weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum.
DOI: 10.1002/mds.20270
PubMed: 15382213
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pubmed:15382213Le document en format XML
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<author><name sortKey="Rocha, N" sort="Rocha, N" uniqKey="Rocha N" first="N" last="Rocha">N. Rocha</name>
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<author><name sortKey="Pinto, M" sort="Pinto, M" uniqKey="Pinto M" first="M" last="Pinto">M. Pinto</name>
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<front><div type="abstract" xml:lang="en">We report on a 54-year-old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2-weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum.</div>
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