Literature DB >> 27072953

Progressive External Ophthalmoplegia.

Collin McClelland1, Georgios Manousakis2, Michael S Lee3,4,5.   

Abstract

Progressive external ophthalmoplegia (PEO), marked by progressive bilateral ptosis and diffuse reduction in ocular motility, represents a finding of mitochondrial myopathy rather than a true diagnosis. PEO often occurs with other systemic features of mitochondrial dysfunction that can cause significant morbidity and mortality. Accurate and early recognition of PEO is paramount for the optimal care of these patients. We present an evidence-based review of the presenting neuro-ophthalmic features, differential diagnosis, diagnostic tools, systemic implications, and treatment options for isolated PEO and other PEO-associated mitochondrial syndromes.

Entities:  

Keywords:  Mitochondrial myopathy; Progressive external ophthalmoplegia

Mesh:

Year:  2016        PMID: 27072953     DOI: 10.1007/s11910-016-0652-7

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  78 in total

1.  CPEO and KSS differ in the percentage and location of the mtDNA deletion.

Authors:  Ester López-Gallardo; Manuel J López-Pérez; Julio Montoya; Eduardo Ruiz-Pesini
Journal:  Mitochondrion       Date:  2009-05-04       Impact factor: 4.160

Review 2.  Recent advances clarifying the etiologies of strabismus.

Authors:  Jason H Peragallo; Stacy L Pineles; Joseph L Demer
Journal:  J Neuroophthalmol       Date:  2015-06       Impact factor: 3.042

3.  Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.

Authors:  Emiliano González-Vioque; Alberto Blázquez; Daniel Fernández-Moreira; Belén Bornstein; Juan Bautista; Javier Arpa; Carmen Navarro; Yolanda Campos; Miguel A Fernández-Moreno; Rafael Garesse; Joaquin Arenas; Miguel A Martín
Journal:  Arch Neurol       Date:  2006-01

4.  Orbital magnetic resonance imaging of extraocular muscles in chronic progressive external ophthalmoplegia: specific diagnostic findings.

Authors:  Maria Carolina Ortube; Rahul Bhola; Joseph L Demer
Journal:  J AAPOS       Date:  2006-10       Impact factor: 1.220

5.  Early retinal involvement in mitochondrial myopathy with mitochondrial DNA deletion.

Authors:  Y Ota; Y Miyake; S Awaya; T Kumagai; M Tanaka; T Ozawa
Journal:  Retina       Date:  1994       Impact factor: 4.256

6.  Single fiber electromyography in chronic progressive external ophthalmoplegia.

Authors:  D A Krendel; D B Sanders; J M Massey
Journal:  Muscle Nerve       Date:  1987-05       Impact factor: 3.217

Review 7.  The in-depth evaluation of suspected mitochondrial disease.

Authors:  Richard H Haas; Sumit Parikh; Marni J Falk; Russell P Saneto; Nicole I Wolf; Niklas Darin; Lee-Jun Wong; Bruce H Cohen; Robert K Naviaux
Journal:  Mol Genet Metab       Date:  2008-02-01       Impact factor: 4.797

8.  OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

Authors:  Patrizia Amati-Bonneau; Maria Lucia Valentino; Pascal Reynier; Maria Esther Gallardo; Belén Bornstein; Anne Boissière; Yolanda Campos; Henry Rivera; Jesús González de la Aleja; Rosanna Carroccia; Luisa Iommarini; Pierre Labauge; Dominique Figarella-Branger; Pascale Marcorelles; Alain Furby; Katell Beauvais; Franck Letournel; Rocco Liguori; Chiara La Morgia; Pasquale Montagna; Maria Liguori; Claudia Zanna; Michela Rugolo; Andrea Cossarizza; Bernd Wissinger; Christophe Verny; Robert Schwarzenbacher; Miguel Angel Martín; Joaquín Arenas; Carmen Ayuso; Rafael Garesse; Guy Lenaers; Dominique Bonneau; Valerio Carelli
Journal:  Brain       Date:  2007-12-24       Impact factor: 13.501

9.  RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy.

Authors:  Aurelio Reyes; Laura Melchionda; Alessia Nasca; Franco Carrara; Eleonora Lamantea; Alice Zanolini; Costanza Lamperti; Mingyan Fang; Jianguo Zhang; Dario Ronchi; Sara Bonato; Gigliola Fagiolari; Maurizio Moggio; Daniele Ghezzi; Massimo Zeviani
Journal:  Am J Hum Genet       Date:  2015-06-18       Impact factor: 11.025

10.  Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease.

Authors:  Cornelia Kornblum; Thomas J Nicholls; Tobias B Haack; Susanne Schöler; Viktoriya Peeva; Katharina Danhauser; Kerstin Hallmann; Gábor Zsurka; Joanna Rorbach; Arcangela Iuso; Thomas Wieland; Monica Sciacco; Dario Ronchi; Giacomo P Comi; Maurizio Moggio; Catarina M Quinzii; Salvatore DiMauro; Sarah E Calvo; Vamsi K Mootha; Thomas Klopstock; Tim M Strom; Thomas Meitinger; Michal Minczuk; Wolfram S Kunz; Holger Prokisch
Journal:  Nat Genet       Date:  2013-01-13       Impact factor: 38.330

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  14 in total

1.  Revisiting mitochondrial ocular myopathies: a study from the Italian Network.

Authors:  D Orsucci; C Angelini; E Bertini; V Carelli; G P Comi; A Federico; C Minetti; M Moggio; T Mongini; F M Santorelli; S Servidei; P Tonin; A Ardissone; L Bello; C Bruno; E Caldarazzo Ienco; D Diodato; M Filosto; C Lamperti; I Moroni; O Musumeci; E Pegoraro; G Primiano; D Ronchi; A Rubegni; S Salvatore; M Sciacco; M L Valentino; L Vercelli; A Toscano; M Zeviani; G Siciliano; M Mancuso
Journal:  J Neurol       Date:  2017-07-10       Impact factor: 4.849

Review 2.  Inherited eye-related disorders due to mitochondrial dysfunction.

Authors:  Patrick Yu-Wai-Man; Nancy J Newman
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

3.  Atheromatosis of the Scalp: A Novel Feature of Chronic Progressive External Ophthalmoplegia Plus Due to a Single Mitochondrial DNA Deletion.

Authors:  Josef Finsterer
Journal:  Cureus       Date:  2021-12-23

4.  Systematic analysis of safety profile for darunavir and its boosted agents using data mining in the FDA Adverse Event Reporting System database.

Authors:  Xiaojiang Tian; Yao Yao; Guanglin He; Yuntao Jia; Kejing Wang; Lin Chen
Journal:  Sci Rep       Date:  2021-06-14       Impact factor: 4.379

Review 5.  Eyelid Dysfunction in Neurodegenerative, Neurogenetic, and Neurometabolic Disease.

Authors:  Ali G Hamedani; Daniel R Gold
Journal:  Front Neurol       Date:  2017-07-18       Impact factor: 4.003

6.  A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma.

Authors:  Triinu Siibak; Paula Clemente; Ana Bratic; Helene Bruhn; Timo E S Kauppila; Bertil Macao; Florian A Schober; Nicole Lesko; Rolf Wibom; Karin Naess; Inger Nennesmo; Anna Wedell; Bradley Peter; Christoph Freyer; Maria Falkenberg; Anna Wredenberg
Journal:  Hum Mol Genet       Date:  2017-07-01       Impact factor: 6.150

Review 7.  Ptosis in childhood: A clinical sign of several disorders: Case series reports and literature review.

Authors:  P Pavone; Sung Yoon Cho; A D Praticò; R Falsaperla; M Ruggieri; Dong-Kyu Jin
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

Review 8.  TWINKLE and Other Human Mitochondrial DNA Helicases: Structure, Function and Disease.

Authors:  Bradley Peter; Maria Falkenberg
Journal:  Genes (Basel)       Date:  2020-04-09       Impact factor: 4.096

9.  Educational Case: Mitochondrial Myopathy.

Authors:  Calixto-Hope G Lucas; Marta Margeta
Journal:  Acad Pathol       Date:  2019-11-29

10.  GWAS Hits for Bilateral Convergent Strabismus with Exophthalmos in Holstein Cattle Using Imputed Sequence Level Genotypes.

Authors:  Anke Bögeholz; Clemens Falker-Gieske; Monika Guélat; Corinne Gurtner; Sibylle Hunziker; Anna Oevermann; Georg Thaller; Cord Drögemüller; Jens Tetens
Journal:  Genes (Basel)       Date:  2021-07-04       Impact factor: 4.096

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