Literature DB >> 25766436

Macular pattern dystrophy and homonymous hemianopia in MELAS syndrome.

Radua Kamal-Salah1, Isabel Baquero-Aranda1, María Del Mar Grana-Pérez1, Jose Manuel García-Campos2.   

Abstract

We report an unusual association of a pattern dystrophy of the retinal pigment epithelium and homonymous hemianopia in a woman diagnosed with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome. 2015 BMJ Publishing Group Ltd.

Entities:  

Mesh：

Year:  2015        PMID： 25766436      PMCID： PMC4368966          DOI： 10.1136/bcr-2014-206499

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


  11 in total

1.  Membrane polarity of the Na(+)-K+ pump in primary cultures of Xenopus retinal pigment epithelium.

Authors:  D M Defoe; A Ahmad; W Chen; B A Hughes
Journal:  Exp Eye Res       Date:  1994-11       Impact factor: 3.467

2.  Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.

Authors:  Y Isashiki; M Nakagawa; N Ohba; K Kamimura; Y Sakoda; I Higuchi; S Izumo; M Osame
Journal:  Acta Ophthalmol Scand       Date:  1998-02

Review 3.  [Eye diseases in mitochondrial encephalomyopathies].

Authors:  D Mojon
Journal:  Ther Umsch       Date:  2001-01

4.  Mitochondrial maculopathy: geographic atrophy of the macula in the MELAS associated A to G 3243 mitochondrial DNA point mutation.

Authors:  P Latkany; T A Ciulla; P F Cacchillo; M D Malkoff
Journal:  Am J Ophthalmol       Date:  1999-07       Impact factor: 5.258

5.  Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group.

Authors:  P Massin; M Virally-Monod; B Vialettes; M Paques; H Gin; B Porokhov; S Caillat-Zucman; P Froguel; V Paquis-Fluckinger; A Gaudric; P J Guillausseau
Journal:  Ophthalmology       Date:  1999-09       Impact factor: 12.079

6.  Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation.

Authors:  C M Sue; P Mitchell; D S Crimmins; C Moshegov; E Byrne; J G Morris
Journal:  Neurology       Date:  1997-10       Impact factor: 9.910

7.  MELAS A3243G mitochondrial DNA mutation and age related maculopathy.

Authors:  Michael Jones; Paul Mitchell; Jie Jin Wang; Carolyn Sue
Journal:  Am J Ophthalmol       Date:  2004-12       Impact factor: 5.258

Review 8.  Mitochondrial DNA (mtDNA) A 3243G mutation associated with an annular perimacular retinal atrophy.

Authors:  E Adjadj; K Mansouri; F-X Borruat
Journal:  Klin Monbl Augenheilkd       Date:  2008-05       Impact factor: 0.700

9.  Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.

Authors:  Terho Latvala; Eila Mustonen; Raimo Uusitalo; Kari Majamaa
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2002-09-21       Impact factor: 3.117

Review 10.  Mitochondrial encephalomyopathies.

Authors:  A Lombes; E Bonilla; S Dimauro
Journal:  Rev Neurol (Paris)       Date:  1989       Impact factor: 2.607
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