You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 63 No. 11, November 2006 TABLE OF CONTENTS
  Archives
  •  Online Features
  Original Contribution
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (3)
 •Contact me when this article is cited
 Related Content
 •Related letters
 •Similar articles in this journal
 Topic Collections
 •Pulmonary Diseases, Other
 •Genetic Disorders
 •Neurogenetics
 •Neuromuscular diseases
 •Neurology, Other
 •Cardiovascular System
 •Cardiovascular Disease/ Myocardial Infarction
 •Alert me on articles by topic

Cardiac and Pulmonary Investigations in Bethlem Myopathy

Anneke J. van der Kooi, MD, PhD; Willem G. de Voogt, MD; Enrico Bertini, MD; Luciano Merlini, MD; F. Beril Talim, MD; Rabah Ben Yaou, MD; Andoni Urtziberea, MD; Marianne de Visser, MD

Arch Neurol. 2006;63:1617-1621.

Background  Bethlem myopathy is considered a relatively mild neuromuscular disorder without significant cardiac and respiratory involvement.

Objective  To investigate cardiac and respiratory involvement in Bethlem myopathy.

Design  Cross-sectional study.

Setting  University hospitals.

Patients  Fifty patients with Bethlem myopathy from 26 families.

Interventions  Cardiac examinations, including electrocardiography and echocardiography (n = 37) and pulmonary investigations (n = 43). Holter monitoring was performed in 16 patients.

Main Outcome Measures  Cardiac and respiratory abnormalities.

Results  Several cardiac abnormalities were found that were considered unrelated to the muscular disorder. Seven (16%) of 43 patients had a forced vital capacity less than 70% of the predicted value. One of 2 patients with a forced vital capacity less than 50% was also receiving respiratory support. All patients with compromised respiratory function were still ambulatory, and we found no significant correlation between the severity of arm weakness and the severity of respiratory muscle involvement.

Conclusions  There is no evidence of cardiac involvement in Bethlem myopathy. Respiratory failure is part of the clinical spectrum and can occur in ambulatory patients.


Author Affiliations: Department of Neurology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands (Drs van der Kooi and de Visser); Department of Cardiology, St Lucas Andreas Hospital, Amsterdam (Dr de Voogt); Unit of Molecular Medicine, Department of Laboratory Medicine, Bambino Gesù Hospital, Rome, Italy (Dr Bertini); Neuromuscular Unit, Division of Medical Genetics, Department of Experimental and Diagnostic Medicine, University of Ferrara, Ferrara, Italy (Dr Merlini); Department of Pediatrics, Hacettepe University, Ankara, Turkey (Dr Talim); and Institut de Myologie, G. H. Pitié Salpetrière, Paris, France (Drs Ben Yaou and Urtziberea).


RELATED LETTERS

Cardiac Involvement in Bethlem Myopathy
Josef Finsterer and Claudia Stöllberger
Arch Neurol. 2007;64(6):915.
EXTRACT | FULL TEXT  

Cardiac Involvement in Bethlem Myopathy—Reply
Anneke J. van der Kooi, Willem G. de Voogt, and Marianne de Visser
Arch Neurol. 2007;64(6):915-916.
EXTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Cardiac Involvement in Bethlem Myopathy
Finsterer and Stollberger
Arch Neurol 2007;64:915-915.
FULL TEXT  

Cardiac Involvement in Bethlem Myopathy--Reply
van der Kooi et al.
Arch Neurol 2007;64:915-916.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2006 American Medical Association. All Rights Reserved.