Literature DB >> 3603608

Frequency of cerebral infarction in patients with inherited neuromuscular diseases.

J Biller, V Ionasescu, H Zellweger, H P Adams, D T Schultz.   

Abstract

We evaluated the frequency of cerebral infarction in 131 patients with Duchenne's muscular dystrophy, myotonic dystrophy, Becker's muscular dystrophy, or Friedreich's ataxia. Electrocardiographic abnormalities were found in 83% of patients with Duchenne's muscular dystrophy, 56% with myotonic dystrophy, 50% with Becker's muscular dystrophy, and 25% with Friedreich's ataxia. Atrial flutter occurred in 2.3% of the patients, and atrial fibrillation in only 0.9%. Evidence of cerebral infarction was found in only 2 patients (1.5%). Both patients had cardiomyopathy and either atrial fibrillation or flutter. Despite frequent cardiac involvement, cerebral infarction is an uncommon occurrence in patients with inherited neuromuscular diseases.

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Year:  1987        PMID: 3603608     DOI: 10.1161/01.str.18.4.805

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  5 in total

1.  Stroke and Stroke-like Episodes in Muscle Disease.

Authors:  Josef Finsterer
Journal:  Open Neurol J       Date:  2012-05-18

2.  Myotonic dystrophy type 1 presenting with stroke-like episodes: a case report.

Authors:  Jens D Rollnik; Ute Heinz; Olaf Lenz
Journal:  BMC Res Notes       Date:  2013-06-26

Review 3.  Fat embolism after fractures in Duchenne muscular dystrophy: an underdiagnosed complication? A systematic review.

Authors:  David Feder; Miriam Eva Koch; Beniamino Palmieri; Fernando Luiz Affonso Fonseca; Alzira Alves de Siqueira Carvalho
Journal:  Ther Clin Risk Manag       Date:  2017-10-10       Impact factor: 2.423

4.  Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey.

Authors:  David C Schorling; Cornelia K Müller; Astrid Pechmann; Sabine Borell; Thorsten Langer; Simone Thiele; Maggie C Walter; Barbara Zieger; Janbernd Kirschner
Journal:  Acta Myol       Date:  2020-03-01

5.  Congenital Muscular Dystrophy due to POMGNT1 Mutation Presenting as Cardioembolic Stroke.

Authors:  Mary Iype; Omana Surendran Mithran; Anitha Ayyappan; Mathew Iype
Journal:  Ann Indian Acad Neurol       Date:  2022-04-25       Impact factor: 1.714

  5 in total

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