Literature DB >> 32395168

Fundus Autofluorescence in Maternally Inherited Diabetes and Deafness: The Gold Standard for Monitoring Maculopathy?

Christopher A Ovens1, Kate Ahmad2, Clare L Fraser3,4.   

Abstract

Maternally inherited diabetes and deafness (MIDD) is a mitochondrial disease associated with dysfunction of the retinal pigment epithelium and photoreceptor outer segments in a peri-foveal arrangement. If chorioretinal atrophy develops, patients risk losing vision. We retrospectively analysed three patients with genetically proven MIDD, assessing atrophy size and progression using overlay in photoshop. Patients showed increase in chorioretinal atrophy of 205%, 46% and 34%, respectively. We also found location-specific progression, where hyper-autofluorescent deposits evolved into areas of atrophy. These results support the use of fundus autofluorescence as a valuable tool in monitoring disease progression and providing prognostic information for clinicians and patients.
© 2019 Taylor & Francis Group, LLC.

Entities:  

Keywords:  Atrophy; MIDD; fundus autofluorescence; maculopathy

Year:  2019        PMID: 32395168      PMCID: PMC7202421          DOI: 10.1080/01658107.2019.1653935

Source DB:  PubMed          Journal:  Neuroophthalmology        ISSN: 0165-8107


  7 in total

1.  Mitochondrial retinal dystrophy associated with the m.3243A>G mutation.

Authors:  Paul de Laat; Jan A M Smeitink; Mirian C H Janssen; Jan E E Keunen; Camiel J F Boon
Journal:  Ophthalmology       Date:  2013-06-24       Impact factor: 12.079

2.  Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.

Authors:  P R Smith; S C Bain; P A Good; A T Hattersley; A H Barnett; J M Gibson; P M Dodson
Journal:  Ophthalmology       Date:  1999-06       Impact factor: 12.079

3.  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

4.  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

5.  Macular pattern dystrophy in MIDD: long-term follow-up.

Authors:  C Ambonville; T Meas; A Lecleire-Collet; M Laloi-Michelin; M Virally; J-P Kevorkian; M Paques; P Massin; P-J Guillausseau
Journal:  Diabetes Metab       Date:  2008-06-30       Impact factor: 6.041

6.  Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.

Authors:  Caren Bellmann; Magella M Neveu; Hendrik P N Scholl; Chris R Hogg; Pamela P Rath; Sharon Jenkins; Alan C Bird; Graham E Holder
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-07       Impact factor: 4.799

Review 7.  Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature.

Authors:  Alejandra Daruich; Alexandre Matet; François-Xavier Borruat
Journal:  BMC Ophthalmol       Date:  2014-06-06       Impact factor: 2.209

  7 in total

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