Literature DB >> 6300733

Chronic progressive external ophthalmoplegia (CPEO): clinical, morphologic, and biochemical studies.

H Mitsumoto, J R Aprille, S H Wray, R Nemni, W G Bradley.   

Abstract

We studied skeletal muscles from eight chronic progressive external ophthalmoplegia patients with ragged-red fibers (group A), five CPEO patients without ragged-red fibers (group B), and five controls. The EM morphometric fraction of structurally abnormal mitochondria was increased in group A, and there was a similarly increased fraction of normal-appearing mitochondria in group B. State 3 respiration and uncoupled respiration were severely decreased in both groups. The morphometric mitochondrial fraction and respiratory functions were inversely related in all three groups. The cytochrome content in group A was normal; cytochromes b and cc1 were decreased in group B. These studies point to a central role of mitochondrial dysfunction in all types of CPEO, but the basic abnormalities remain to be elucidated.

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Year:  1983        PMID: 6300733     DOI: 10.1212/wnl.33.4.452

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  16 in total

1.  Human quadriceps muscle mitochondria: a functional characterization.

Authors:  U F Rasmussen; H N Rasmussen
Journal:  Mol Cell Biochem       Date:  2000-05       Impact factor: 3.396

2.  Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

Authors:  D M Slipetz; J R Aprille; P R Goodyer; R Rozen
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

3.  Skeletal muscle pathology in chronic progressive external ophthalmoplegia with ragged-red fibers.

Authors:  M Yamamoto; I Nonaka
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

4.  Morphometric and biochemical study of muscle mitochondria in adult chronic progressive external ophthalmoplegia.

Authors:  A Federico; L Manneschi; P Sabatelli; M T Dotti; G Ciacci; L Ibba; R Gerli
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

5.  Retinal pathology in the Kearns-Sayre syndrome.

Authors:  N M McKechnie; M King; W R Lee
Journal:  Br J Ophthalmol       Date:  1985-01       Impact factor: 4.638

Review 6.  Morphological observations in skeletal muscle from patients with a mitochondrial myopathy.

Authors:  A M Stadhouders; R C Sengers
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

7.  Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia.

Authors:  A Schaller; R Desetty; D Hahn; C B Jackson; J-M Nuoffer; S Gallati; L Levinger
Journal:  Mitochondrion       Date:  2011-02-01       Impact factor: 4.160

8.  Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus.

Authors:  S Zierz; G Jahns; F Jerusalem
Journal:  J Neurol       Date:  1989-02       Impact factor: 4.849

9.  Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutation.

Authors:  Michael K Yoon; Austin Roorda; Yuhua Zhang; Chiaki Nakanishi; Lee-Jun C Wong; Qing Zhang; Leslie Gillum; Ari Green; Jacque L Duncan
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-11-07       Impact factor: 4.799

Review 10.  Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and non-hereditary neuropathies, and review of the literature.

Authors:  J M Schröder; C Sommer
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

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