Myopathies mitochondriales oculaires: un eventail de presentations cliniques. [Ocular mitochondrial myopathies: a spectrum of clinical presentations]

Details

Serval ID
serval:BIB_227DADE19E0D
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Myopathies mitochondriales oculaires: un eventail de presentations cliniques. [Ocular mitochondrial myopathies: a spectrum of clinical presentations]
Journal
Klinische Monatsblatter fur Augenheilkunde
Author(s)
Glutz von Blotzheim  S., Borruat  F. X., Hirt  L.
ISSN
0023-2165 (Print)
Publication state
Published
Issued date
05/1998
Volume
212
Number
5
Pages
299-300
Notes
English Abstract
Journal Article --- Old month value: May
Abstract
PURPOSE: To determine the spectrum of clinical presentations of patients with chronic progressive external ophthalmoplegia (CPEO). METHODS: Retrospective study of 13 cases with CPEO. RESULTS: Eight patients presented an isolated CPEO, three patients had an associated retinopathy (Kearns-Sayre syndrome), one case suffered from retinopathy, deafness, diabetes mellitus and dysphagia, and one patient had an associated dysphagia. Mitochondrial DNA deletions were found in two cases. CONCLUSIONS: Our cases illustrate the wide spectrum of mitochondrial ocular myopathies. As patients present mostly with ptosis and ophthalmoplegia, ophthalmologists should be aware of these rare conditions.
Keywords
Adult Chromosome Deletion DNA, Mitochondrial/genetics Female Humans Kearns-Sayer Syndrome/*diagnosis/genetics Male Ophthalmoplegia, Chronic Progressive External/*diagnosis/genetics Retrospective Studies
Pubmed
Create date
28/01/2008 13:37
Last modification date
20/08/2019 13:59
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