Literature DB >> 1954213

Persistent superior oblique paresis as a manifestation of familial periodic cerebellar ataxia.

P G Bain1, G B Larkin, D M Calver, M D O'Brien.   

Abstract

A brother and sister complained of persistent diplopia due to superior oblique palsies. The cause of their symptoms became apparent when they were diagnosed as having familial periodic cerebellar ataxia (FPCA), a rare autosomal dominant condition. Oral acetazolamide (250 mg twice daily) not only prevented all the periodic symptoms but also relieved their diplopia, which had been present between attacks.

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Year:  1991        PMID: 1954213      PMCID: PMC1042501          DOI: 10.1136/bjo.75.10.619

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  10 in total

Review 1.  Acetazolamide responsive hereditary paroxysmal ataxia.

Authors:  J H Friedman; P A Hollmann
Journal:  Mov Disord       Date:  1987       Impact factor: 10.338

2.  Hereditary paroxysmal ataxia: response to acetazolamide.

Authors:  R C Griggs; R T Moxley; R A Lafrance; J McQuillen
Journal:  Neurology       Date:  1978-12       Impact factor: 9.910

3.  Acute intermittent familial cerebellar ataxia.

Authors:  W Hill; H Sherman
Journal:  Arch Neurol       Date:  1968-04

4.  Familial periodic nystagmus, vertigo, and ataxia.

Authors:  J C White
Journal:  Arch Neurol       Date:  1969-03

5.  Familial periodic ataxia responsive to acetazolamide.

Authors:  J P Bouchard; C Roberge; N M van Gelder; A Barbeau
Journal:  Can J Neurol Sci       Date:  1984-11       Impact factor: 2.104

6.  Familial intermittent ataxia with possible X-linked recessive inheritance. Two patients with abnormal pyruvate metabolism and a response to acetazolamide.

Authors:  I R Livingstone; D Gardner-Medwin; R J Pennington
Journal:  J Neurol Sci       Date:  1984-04       Impact factor: 3.181

7.  [Familial paroxysmal ataxia responsive to acetazolamide].

Authors:  G Aimard; A Vighetto; M Trillet; J J Ventre; M Devic
Journal:  Rev Neurol (Paris)       Date:  1983       Impact factor: 2.607

8.  [Familial paroxysmal ataxia sensitive to acetazolamide. 3 cases in a new European family].

Authors:  M Trillet; M Gouttard; B Schott
Journal:  Rev Neurol (Paris)       Date:  1985       Impact factor: 2.607

9.  Acetazolamide-responsive episodic ataxia syndrome.

Authors:  N L Zasorin; R W Baloh; L B Myers
Journal:  Neurology       Date:  1983-09       Impact factor: 9.910

10.  Familial periodic ataxia.

Authors:  J R Donat; R Auger
Journal:  Arch Neurol       Date:  1979-09
  10 in total
  2 in total

Review 1.  Diagnosis and management of acute movement disorders.

Authors:  D Dressler; R Benecke
Journal:  J Neurol       Date:  2005-10-10       Impact factor: 4.849

2.  Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia.

Authors:  D S McCorquodale; U Ozomaro; J Huang; G Montenegro; A Kushman; L Citrigno; J Price; F Speziani; M A Pericak-Vance; S Züchner
Journal:  Clin Genet       Date:  2011-06       Impact factor: 4.438

  2 in total

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