Literature DB >> 1592574

Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan.

F Salvi1, R Michelucci, R Plasmati, L Parmeggiani, P Zonari, M Mascalchi, C A Tassinari.   

Abstract

We describe 2 normotensive sisters presenting slowly progressive dementia associated with acute or subacute focal neurological symptoms, unilateral or bilateral motor signs, and dysarthria. Their father, who died in the seventh decade, had a similar clinical picture. Computerized axial tomography (CT) scan of the head showed symmetrical hypodensities in the periventricular white matter and mild to moderate hydrocephalus. In these patients a diagnosis of Binswanger's disease was based on the clinical features supported by white matter changes on CT scan. Our study suggests that genetic factors may play a role in the etiology of Binswanger's disease.

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Year:  1992        PMID: 1592574     DOI: 10.1007/bf02226962

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  22 in total

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Journal:  Brain       Date:  1972       Impact factor: 13.501

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Journal:  Folia Psychiatr Neurol Jpn       Date:  1976

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Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-05       Impact factor: 10.154

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Journal:  Neurology       Date:  1979-08       Impact factor: 9.910

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Journal:  J Comput Assist Tomogr       Date:  1980-02       Impact factor: 1.826

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Journal:  Neurology       Date:  1978-12       Impact factor: 9.910

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Journal:  J Exp Med       Date:  1983-08-01       Impact factor: 14.307

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  6 in total

1.  Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity.

Authors:  D St Clair; J Bolt; S Morris; D Doyle
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

2.  New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature.

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Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-12       Impact factor: 10.154

3.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.

Authors:  A Ducros; T Nagy; S Alamowitch; A Nibbio; A Joutel; K Vahedi; H Chabriat; M T Iba-Zizen; J Julien; P Davous; J Y Goas; O Lyon-Caen; B Dubois; X Ducrocq; F Salsa; M Ragno; P Burkhard; C Bassetti; M Hutchinson; M Vérin; F Viader; F Chapon; M Levasseur; J L Mas; O Delrieu
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

4.  Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Authors:  J M Schröder; B Sellhaus; J Jörg
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

5.  Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  M M Ruchoux; D Guerouaou; B Vandenhaute; J P Pruvo; P Vermersch; D Leys
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

6.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.

Authors:  H H Jung; C Bassetti; E Tournier-Lasserve; K Vahedi; M Arnaboldi; V B Arifi; J M Burgunder
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

  6 in total

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