Literature DB >> 21898092

Topiramate and visual loss in a patient carrying a Leber hereditary optic neuropathy mutation.

Steno Rinalduzzi1, Anna Maria Cipriani, Neri Accornero.   

Abstract

We describe a 43-year-old patient who experienced visual loss 4 years after beginning antiepileptic therapy with topiramate. Ophthalmological and neurological examinations led to a preliminary diagnosis of bilateral toxic optic neuritis. Mitochondrial genome sequence analysis detected a Leber hereditary optic neuropathy 11778G>A mutation. The possibility that topiramate might favor a conversion disease, alerts physicians to seek a history of blindness in patients undergoing chronic antiepileptic therapy.

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Year:  2011        PMID: 21898092     DOI: 10.1007/s10072-011-0755-5

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.307


  12 in total

1.  Retinal function and histopathology in rabbits treated with Topiramate.

Authors:  S Kjellström; A Bruun; B Isaksson; T Eriksson; S Andréasson; V Ponjavic
Journal:  Doc Ophthalmol       Date:  2006-11-18       Impact factor: 2.379

2.  Closed-angle glaucoma after topiramate therapy for migraine in a patient with undiagnosed pseudotumor cerebri.

Authors:  Gian P Giuliari; Rodolfo M Banda; Vincent R Vann; Victor H Gonzalez; Reagan B McMillin
Journal:  Can J Ophthalmol       Date:  2008-06       Impact factor: 1.882

3.  Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.

Authors:  Liesbeth Spruijt; Dinanda N Kolbach; Rene F de Coo; Astrid S Plomp; Noel J Bauer; Hubertus J Smeets; Christine E M de Die-Smulders
Journal:  Am J Ophthalmol       Date:  2006-04       Impact factor: 5.258

4.  Changes in color vision after a single dose of vigabatrin or carbamazepine in healthy volunteers.

Authors:  O Mecarelli; S Rinalduzzi; N Accornero
Journal:  Clin Neuropharmacol       Date:  2001 Jan-Feb       Impact factor: 1.592

5.  The influence of established and new antiepileptic drugs on visual perception. II. A controlled study in patients with epilepsy under long-term antiepileptic medication.

Authors:  B J Steinhoff; N Freudenthaler; W Paulus
Journal:  Epilepsy Res       Date:  1997-12       Impact factor: 3.045

Review 6.  Leber hereditary optic neuropathy.

Authors:  P Yu-Wai-Man; D M Turnbull; P F Chinnery
Journal:  J Med Genet       Date:  2002-03       Impact factor: 6.318

7.  Electronegative electroretinogram associated with topiramate toxicity and vitelliform maculopathy.

Authors:  Irena Tsui; Daniel Casper; Chai Lin Chou; Stephen H Tsang
Journal:  Doc Ophthalmol       Date:  2007-10-03       Impact factor: 2.379

Review 8.  The effect of antiepileptic drugs on visual performance.

Authors:  Emma J Roff Hilton; Sarah L Hosking; Tim Betts
Journal:  Seizure       Date:  2004-03       Impact factor: 3.184

9.  Gene-environment interactions in Leber hereditary optic neuropathy.

Authors:  Matthew Anthony Kirkman; Patrick Yu-Wai-Man; Alex Korsten; Miriam Leonhardt; Konstantin Dimitriadis; Ireneaus F De Coo; Thomas Klopstock; Patrick Francis Chinnery
Journal:  Brain       Date:  2009-06-12       Impact factor: 13.501

Review 10.  Inherited mitochondrial optic neuropathies.

Authors:  P Yu-Wai-Man; P G Griffiths; G Hudson; P F Chinnery
Journal:  J Med Genet       Date:  2008-11-10       Impact factor: 6.318

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  4 in total

Review 1.  Effects of Topiramate on afferent visual pathways: controversies and uncertainties.

Authors:  Seyed-Hossein Abtahi; Mohammad-Ali Abtahi; Masoud Etemadifar; Mehdi Mazloumi; Hossein Attarzadeh
Journal:  Neurol Sci       Date:  2012-05-19       Impact factor: 3.307

2.  Response to: Letter to the Editor regarding: The expanding phenotype of MELAS caused by the m.3291T > C tRNA mutation E. Kelland, C.A. Rupar, Asuri N. Prasad, A. Downie and C. Prasad (1) by Josef Finsterer, MD, PhD [1], Sinda Zarrouk-Mahjoub, PhD [2].

Authors: 
Journal:  Mol Genet Metab Rep       Date:  2016-06-01

3.  Sulthiame impairs mitochondrial function in vitro and may trigger onset of visual loss in Leber hereditary optic neuropathy.

Authors:  Marie-Christine Reinert; David Pacheu-Grau; Claudia B Catarino; Thomas Klopstock; Andreas Ohlenbusch; Michael Schittkowski; Ekkehard Wilichowski; Peter Rehling; Knut Brockmann
Journal:  Orphanet J Rare Dis       Date:  2021-02-04       Impact factor: 4.123

4.  MELAS syndrome due to the m.3291T > C mutation.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Mol Genet Metab Rep       Date:  2016-04-13
  4 in total

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