Two sisters with generalized dystonia associated with homocystinuria

A. Berardelli; P. D. Thompson; M. Zaccagnini; O. Giardini; P. D'Eufemia; R. Massoud; M. Manfredi

Two sisters with generalized dystonia associated with homocystinuria

A. Berardelli, P. D. Thompson, M. Zaccagnini, O. Giardini, P. D'Eufemia, R. Massoud, M. Manfredi

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Abstract

Two sisters with progressive dystonic syndromes and homocystinuria are presented. The biochemical defect was not accompanied by the typical clinical features of homocystinuria. Magnetic resonance imaging (MRI) revealed bilateral lesions of the basal ganglia. Homocystinuria should be considered among the causes of symptomatic or secondary dystonias associated with basal ganglia lesions.

Original language	English
Pages (from-to)	163-165
Number of pages	3
Journal	Movement Disorders
Volume	6
Issue number	2
Publication status	Published - 1991

ASJC Scopus subject areas

Clinical Neurology
Neuroscience(all)

Cite this

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title = "Two sisters with generalized dystonia associated with homocystinuria",

abstract = "Two sisters with progressive dystonic syndromes and homocystinuria are presented. The biochemical defect was not accompanied by the typical clinical features of homocystinuria. Magnetic resonance imaging (MRI) revealed bilateral lesions of the basal ganglia. Homocystinuria should be considered among the causes of symptomatic or secondary dystonias associated with basal ganglia lesions.",

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AU - Berardelli, A.

AU - Thompson, P. D.

AU - Zaccagnini, M.

AU - Giardini, O.

AU - D'Eufemia, P.

AU - Massoud, R.

AU - Manfredi, M.

PY - 1991

Y1 - 1991

N2 - Two sisters with progressive dystonic syndromes and homocystinuria are presented. The biochemical defect was not accompanied by the typical clinical features of homocystinuria. Magnetic resonance imaging (MRI) revealed bilateral lesions of the basal ganglia. Homocystinuria should be considered among the causes of symptomatic or secondary dystonias associated with basal ganglia lesions.

AB - Two sisters with progressive dystonic syndromes and homocystinuria are presented. The biochemical defect was not accompanied by the typical clinical features of homocystinuria. Magnetic resonance imaging (MRI) revealed bilateral lesions of the basal ganglia. Homocystinuria should be considered among the causes of symptomatic or secondary dystonias associated with basal ganglia lesions.

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JO - Movement Disorders

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Two sisters with generalized dystonia associated with homocystinuria

Abstract

ASJC Scopus subject areas

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