Rehabilitation of a Patient with Neutral Lipid Storage Disease with Myopathy and Triglyceride Deposit Cardiomyovasculopathy : a Case Report
Author:
Affiliation:
1. Department of Internal Medicine and Rehabilitation Science, Tohoku University Graduate School of Medicine
2. Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine
Publisher
Japanese Association of Rehabilitation Medicine
Link
https://www.jstage.jst.go.jp/article/jjrmc/53/6/53_495/_pdf
Reference10 articles.
1. 1) Fischer J, Lefevre C, Morava E, Mussini JM, Laforet P, Negre-Salvayre A, Lathrop M, Salvayre R:The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy. Nat Genet 2007;39:28-30
2. 2) Hirano K, Ikeda Y, Zaima N, Sakata Y, Matsumiya G:Triglyceride deposit cardiomyovasculopathy. N Engl J Med 2008;359:2396-2398
3. 4) Huijsman E, van de Par C, Economou C, van der Poel C, Lynch GS, Schoiswohl G, Haemmerle G, Zechner R, Watt MJ:Adipose triacylglycerol lipase deletion alters whole body energy metabolism and impairs exercise performance in mice. Am J Physiol Endocrinol Metab 2009;297:E505-513
4. 7) Working Group on Cardiac Rehabilitation & Exercise Physiology and Working Group on Heart Failure of the European Society of Cardiology. Recommendations for exercise training in chronic heart failure patients. Eur Heart J 2001;22:125-135
5. 8) Schweiger M, Lass A, Zimmermann R, Eichmann TO, Zechner R:Neutral lipid storage disease genetic disorders caused by mutations in adipose triglyceride lipase/PNPLA2 or CGI-58/ABHD5. Am J Physiol Endocrinol Metab 2009;297:E289-296
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