Literature DB >> 20882363

Late-onset progressive visual loss in a man with unusual MRI findings: MS, Harding's, Leber's or Leber's Plus?

N Cawley1, A Molloy, L Cassidy, N Tubridy.   

Abstract

Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder, typically presenting in the second and third decade. We report the case of an elderly gentleman with significant vascular risk factors, presenting with slowly progressive, bilateral, visual loss with high signal lesions in the pericallosal and periventricular deep white matter on MRI brain studies. Possible diagnoses included late-onset MS, ischaemic optic neuropathies, a mitochondrial disorder or an overlap syndrome such as Harding's disease.

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Year:  2010        PMID: 20882363     DOI: 10.1007/s11845-010-0586-z

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  9 in total

1.  Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

Authors:  L Vanopdenbosch; B Dubois; M B D'Hooghe; F Meire; H Carton
Journal:  J Neurol       Date:  2000-07       Impact factor: 4.849

2.  White matter changes in Leber's hereditary optic neuropathy: MRI findings.

Authors:  W Küker; A Weir; G Quaghebeur; J Palace
Journal:  Eur J Neurol       Date:  2007-05       Impact factor: 6.089

3.  Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.

Authors:  Simona D'Aguanno; Alessandra Barassi; Santina Lupisella; Gianlodovico Melzi d'eril; Piero Del Boccio; Damiana Pieragostino; Francesco Pallotti; Valerio Carelli; Maria Lucia Valentino; Rocco Liguori; Patrizia Avoni; Sergio Bernardini; Domenico Gambi; Andrea Urbani; Giorgio Federici
Journal:  J Neuroimmunol       Date:  2007-12-03       Impact factor: 3.478

4.  Leber's hereditary optic neuropathy associated with multiple sclerosis: Harding's syndrome.

Authors:  A R Parry-Jones; J D Mitchell; W J Gunarwardena; S Shaunak
Journal:  Pract Neurol       Date:  2008-04

Review 5.  [Past, present, and future in Leber's hereditary optic neuropathy].

Authors:  Y Oguchi
Journal:  Nippon Ganka Gakkai Zasshi       Date:  2001-12

Review 6.  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

7.  Neuropathology of white matter disease in Leber's hereditary optic neuropathy.

Authors:  Gábor G Kovács; Romana Höftberger; Katalin Majtényi; Rita Horváth; Péter Barsi; Sámuel Komoly; Hans Lassmann; Herbert Budka; Gábor Jakab
Journal:  Brain       Date:  2004-10-13       Impact factor: 13.501

8.  Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

Authors:  R J Oostra; P A Bolhuis; F A Wijburg; G Zorn-Ende; E M Bleeker-Wagemakers
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

9.  Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

Authors:  E K Nikoskelainen; R J Marttila; K Huoponen; V Juvonen; T Lamminen; P Sonninen; M L Savontaus
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

  9 in total

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