Literature DB >> 18429762

[Peculiarities of cardiac involvement in patients with dystrophic myotonia].

V A Shul'man1, N A Shnaĭder, E A Kozulina, R A But'ianov, L A Sviderskaia.   

Abstract

Dystrophic myotonia is a widespread hereditary disease. Pathological process touches development and functioning of various organs and tissues: smooth and skeletal muscular tissue, the heart, organ of vision, brain. Pathology of the heart serves as one of frequent manyfestations of dystrophic myotonia. Degenerative changes and fatty infiltration of myocardium not infrequently leads to dilated cardiomyopathy. Involvement of the heart in such patients is represented mainly by disturbance of cardiac rhythm and conduction. Course of the disease is progressive.

Entities:  

Mesh:

Year:  2008        PMID: 18429762

Source DB:  PubMed          Journal:  Kardiologiia        ISSN: 0022-9040            Impact factor:   0.395


  1 in total

1.  Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders.

Authors:  Linda L Bachinski; Mario Sirito; Maria Böhme; Keith A Baggerly; Bjarne Udd; Ralf Krahe
Journal:  Muscle Nerve       Date:  2010-12       Impact factor: 3.217

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.