Journal article
Childhood Onset Inclusion Body Myositis Mimicking Limb-Girdle Muscular Dystrophy
Journal of child neurology, Vol.4(4), pp.283-285
10/1989
DOI: 10.1177/088307388900400406
PMID: 2551952
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).
Details
- Title: Subtitle
- Childhood Onset Inclusion Body Myositis Mimicking Limb-Girdle Muscular Dystrophy
- Creators
- Jack E Riggs - Departments of Neurology and Pathology, West Virginia University School of Medicine, Morgantown, WVSydney S Schochet - Departments of Neurology and Pathology, West Virginia University School of Medicine, Morgantown, WVLudwig Gutmann - Departments of Neurology and Pathology, West Virginia University School of Medicine, Morgantown, WVSidney C Lerfald - Departments of Neurology and Pathology, West Virginia University School of Medicine, Morgantown, WV
- Resource Type
- Journal article
- Publication Details
- Journal of child neurology, Vol.4(4), pp.283-285
- Publisher
- Sage Publications; Thousand Oaks, CA
- DOI
- 10.1177/088307388900400406
- PMID
- 2551952
- ISSN
- 0883-0738
- eISSN
- 1708-8283
- Language
- English
- Date published
- 10/1989
- Academic Unit
- Neurology
- Record Identifier
- 9984020505502771
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