Childhood Onset Inclusion Body Myositis Mimicking Limb-Girdle Muscular Dystrophy-Reference-Cited by-同舟云学术

Childhood Onset Inclusion Body Myositis Mimicking Limb-Girdle Muscular Dystrophy

Published:1989-10 Issue:4 Volume:4 Page:283-285
ISSN:0883-0738
Container-title:Journal of Child Neurology
language:en
Short-container-title:J Child Neurol

Author:

Riggs Jack E.¹,Schochet Sydney S.¹,Gutmann Ludwig¹,Lerfald Sidney C.¹

Affiliation:

1. Departments of Neurology and Pathology, West Virginia University School of Medicine, Morgantown, WV

Abstract

Inclusion body myositis was initially recognized in patients with "steroid-resistant polymyositis" and subsequently in patients with other immune-mediated disorders. The finding of inclusion body myositis in a patient diagnosed for 30 years as having limb-girdle muscular dystrophy suggests yet another patient pool that may harbor this entity. ( J Child Neurol 1989;4:283-285).

Publisher

SAGE Publications

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/088307388900400406

Reference16 articles.

1. Myxovirus-Like Structures in a Case of Human Chronic Polymyositis

2. Inclusion body myositis: A distinct variety of idiopathic inflammatory myopathy

3. Inclusion Body Myositis

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