Literature DB >> 3711913

Familial dystonia and visual failure with striatal CT lucencies.

C D Marsden, A E Lang, N P Quinn, W I McDonald, A Abdallat, S Nimri.   

Abstract

A unique disorder is described in seven members of two families in whom dystonia was variably associated with subacute visual loss or asymptomatic optic atrophy, and striking bilateral symmetrical lucencies on CT scan, especially involving the putamen. It is possible that this is a variant of Leigh's disease. However, there were considerable differences between these patients and those with pathologically proven Leigh's disease. This condition must be excluded in all patients thought to have idiopathic dystonia, subacute visual failure similar to Leber's optic neuropathy, or a combination of these disorders.

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Year:  1986        PMID: 3711913      PMCID: PMC1028803          DOI: 10.1136/jnnp.49.5.500

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  41 in total

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Journal:  Acta Paediatr       Date:  1956-07       Impact factor: 2.299

2.  Subacute necrotizing encephalomyelopathy (Leigh's disease): a consideration of clinical features and etiology.

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Journal:  Dev Med Child Neurol       Date:  1972-02       Impact factor: 5.449

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Authors:  E Nikoskelainen; R L Sogg; A R Rosenthal; T R Friberg; L J Dorfman
Journal:  Arch Ophthalmol       Date:  1977-06

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Authors:  D Meek; L S Wolfe; E Andermann; F Andermann
Journal:  Ann Neurol       Date:  1984-04       Impact factor: 10.422

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Authors:  D Yashon; J A Jane
Journal:  J Clin Pathol       Date:  1967-01       Impact factor: 3.411

6.  Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features.

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Journal:  Ann Neurol       Date:  1981-05       Impact factor: 10.422

7.  Injuries of basal ganglia following head trauma in children.

Authors:  Y Maki; H Akimoto; T Enomoto
Journal:  Childs Brain       Date:  1980

8.  [Extrapyramidal rigidity with dystonia, optic atrophy and bilateral putaminal lesions in an adolescent. Juvenile form of Leigh's disease (author's transl)].

Authors:  P Rondot; J de Recondo; P Davous; D Fredy; F X Roux
Journal:  Rev Neurol (Paris)       Date:  1982       Impact factor: 2.607

9.  A pure parkinsonian syndrome following acute carbon monoxide intoxication.

Authors:  H L Klawans; R W Stein; C M Tanner; C G Goetz
Journal:  Arch Neurol       Date:  1982-05

10.  Hypertrophic cardiomyopathy is a component of subacute necrotizing encephalomyelopathy.

Authors:  J C Rutledge; J E Haas; R Monnat; J M Milstein
Journal:  J Pediatr       Date:  1982-11       Impact factor: 4.406

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  11 in total

1.  Bilateral striatal necrosis, dystonia and optic atrophy in two siblings.

Authors:  V Leuzzi; E Bertini; A M De Negri; M Gallucci; B Garavaglia
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-01       Impact factor: 10.154

2.  Characterization of basal ganglia dysfunction in Leber 'plus' disease.

Authors:  C O Hanemann; H Hefter; G Schlaug; R J Seitz; H J Freund; R Benecke
Journal:  J Neurol       Date:  1996-03       Impact factor: 4.849

3.  Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.

Authors:  A S Jun; I A Trounce; M D Brown; J M Shoffner; D C Wallace
Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

Review 4.  The genetics of primary torsion dystonia.

Authors:  U Müller; K G Kupke
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

Review 5.  Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.

Authors:  P Riordan-Eva; A E Harding
Journal:  J Med Genet       Date:  1995-02       Impact factor: 6.318

6.  Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system?

Authors:  D Caparros-Lefebvre; A Destee; H Petit
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-08       Impact factor: 10.154

7.  Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

Authors:  D D De Vries; L N Went; G W Bruyn; H R Scholte; R M Hofstra; P A Bolhuis; B A van Oost
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

8.  Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.

Authors:  Kang Wang; Yuji Takahashi; Zong-Liang Gao; Guo-Xiang Wang; Xian-Wen Chen; Jun Goto; Jin-Ning Lou; Shoji Tsuji
Journal:  Neurogenetics       Date:  2009-05-21       Impact factor: 2.660

9.  A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.

Authors:  R S Howard; R Greenwood; J Gawler; F Scaravilli; C D Marsden; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-09       Impact factor: 10.154

10.  A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.

Authors:  A S Jun; M D Brown; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205

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