Literature DB >> 7307870

Ophthalmoplegia-plus.

V Godel, P Nemet, I Reider-Groswasser, G Messer, M Lazar.   

Abstract

The occurrence of chronic progressive external ophthalmoplegia, pigmentary retinal dystrophy and cardiac disturbances associated with arachnodactily, sternal deformity, high arched palate and severe myopia is reported. A pedigree analysis of this Jewish-Iranian family strongly suggests that the condition is inherited as autosomal recessive trait. The terminology of the condition and the spectrum of it variable phenotypic expression is described.

Entities:  

Mesh:

Year:  1981        PMID: 7307870     DOI: 10.1007/bf00143339

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  20 in total

1.  Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases.

Authors:  T P KEARNS; G P SAYRE
Journal:  AMA Arch Ophthalmol       Date:  1958-08

2.  Ophthalmoplegia-plus, a real nosological entity.

Authors:  L A Bastiaensen; E M Joosten; J A de Rooij; O R Hommes; A M Stadhouders; H H Jaspar; J H Veerkamp; H Bookelman; V W van Hinsbergh
Journal:  Acta Neurol Scand       Date:  1978-07       Impact factor: 3.209

3.  External Ophthalmoplegia, Pigmentary Degeneration of the Retina, and Cardiomyopathy: A Newly Recognized Syndrome.

Authors:  T P Kearns
Journal:  Trans Am Ophthalmol Soc       Date:  1965

4.  Familial progressive external ophthalmoplegia with abnormal muscle mitochondria.

Authors:  E Jankowicz; H Berger; S Kurasz; W Winogrodzka; L Eljasz
Journal:  Eur Neurol       Date:  1977       Impact factor: 1.710

5.  Pigment changes of the retina in chronic progressive external ophthalmoplegia (CPEO).

Authors:  L A Bastiaensen
Journal:  Acta Ophthalmol Suppl       Date:  1978

6.  Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia.

Authors:  D A Drachman
Journal:  Arch Neurol       Date:  1968-06

7.  Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia.

Authors:  M Adachi; J Torii; B W Volk; P Briet; A Wolintz; L Schneck
Journal:  Acta Neuropathol       Date:  1973       Impact factor: 17.088

8.  Familial Kearns-Sayre syndrome.

Authors:  E R Schnitzler; W C Robertson
Journal:  Neurology       Date:  1979-08       Impact factor: 9.910

9.  Autosomal dominant Kearns-Sayre syndrome.

Authors:  A S Leveille; F W Newell
Journal:  Ophthalmology       Date:  1980-02       Impact factor: 12.079

10.  Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy.

Authors:  G M Shy; N K Gonatas; M Perez
Journal:  Brain       Date:  1966-03       Impact factor: 13.501

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