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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/51583
Title: Concurrent positive anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase antibody with reducing body myopathy: Possible double trouble
Authors: Jantima Tanboon
Oranee Sanmaneechai
Sirirat Charuvanij
Tumtip Sangruchi
Angeles S. Galindo-Feria
Ingrid E. Lundberg
Yuko Ohnuki
Takashi Shiina
Shigeaki Suzuki
Ichizo Nishino
Tokai University School of Medicine
Keio University School of Medicine
National Institute of Neuroscience, Kodaira
Karolinska University Hospital
National Center of Neurology and Psychiatry Kodaira
Faculty of Medicine, Siriraj Hospital, Mahidol University
Keywords: Medicine
Issue Date: 1-Jul-2019
Citation: Neuromuscular Disorders. Vol.29, No.7 (2019), 543-548
Abstract: © 2019 Elsevier B.V. Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase myopathy is less common in children but has been associated with more favorable prognosis than adult patients after immunotherapies. We report anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibody positivity in a 6-year-old boy with progressive muscle weakness, scoliosis, spinal rigidity, multiple joint contractures, mild left ventricular hypertrophy, and elevated serum creatine kinase. In contrast to most of previously reported pediatric anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase myopathy, he showed little response to immunotherapies. Muscle biopsy contained changes suggestive of myofiber necrosis and regeneration and reducing bodies. The diagnosis of reducing body myopathy was later confirmed by reported c.368A>G (p.His123Arg) mutation in the FHL1 gene. Although the level of association between these two conditions is still inconclusive, this is the first report of concurrent positive anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibody with reducing body myopathy emphasizing the possibility of co-occurrence of immune mediated necrotizing myopathy and muscular dystrophy and importance of comprehensive diagnostic investigations in unusual cases.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/51583
metadata.dc.identifier.url: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067210853&origin=inward
ISSN: 18732364
09608966
Appears in Collections:Scopus 2019

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