Literature DB >> 3336450

Mineralization of the basal ganglia detected by CT in Hallervorden-Spatz syndrome.

M B Tennison1, T W Bouldin, R A Whaley.   

Abstract

We studied a patient with autopsy-proven Hallervorden-Spatz syndrome (HSS) and the previously unreported finding of high-density lesions in the basal ganglia on CT. The diagnosis of HSS should be considered in a patient with dystonia and basal ganglia mineralization on CT.

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Year:  1988        PMID： 3336450     DOI： 10.1212/wnl.38.1.154

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


  3 in total

1.  Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life.

Authors:  L Angelini; N Nardocci; V Rumi; C Zorzi; L Strada; M Savoiardo
Journal:  J Neurol       Date:  1992-10       Impact factor: 4.849

2.  Early clinical and imaging (high-field MRI) diagnosis of Hallervorden-Spatz disease.

Authors:  M Feliciani; P Curatolo
Journal:  Neuroradiology       Date:  1994-04       Impact factor: 2.804

Review 3.  Neuropathology in movement disorders.

Authors:  W R Gibb
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-06       Impact factor: 10.154
  3 in total

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