Literature DB >> 2411500

Identification of minimal expression of myotonic dystrophy using electroretinography.

D J Creel, A S Crandall, F A Ziter.   

Abstract

The electroretinograms (ERGs) of patients with definite myotonic dystrophy were studied as well as neurologically asymptomatic patients with minimal expression of myotonic dystrophy. Children in 4 families exhibited definite myotonic dystrophy when neither parent exhibited clinical or electromyographic signs of myotonic dystrophy. Myotonic dystrophy is dominantly inherited. We were able to identify the asymptomatic parent with the gene in these families. This study suggests that ERG testing, which includes scotopically balanced dim blue and red flashes, will identify some asymptomatic adults minimally expressing the gene for myotonic dystrophy.

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Year:  1985        PMID: 2411500     DOI: 10.1016/0013-4694(85)91088-0

Source DB:  PubMed          Journal:  Electroencephalogr Clin Neurophysiol        ISSN: 0013-4694


  2 in total

1.  Foveal photopigment kinetics--abnormality: an early sign in myotonic dystrophy?

Authors:  J P ter Bruggen; G J van Meel; A D Paridaens; C C Tijssen; D van Norren
Journal:  Br J Ophthalmol       Date:  1992-10       Impact factor: 4.638

2.  Reader response: Consensus-based care recommendations for adults with myotonic dystrophy type 1.

Authors:  Tuy Nga Brignol; Patrice E Fort
Journal:  Neurol Clin Pract       Date:  2019-10
  2 in total

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