Literature DB >> 9588538

Hypertrophic cardiomyopathy in congenital myotonic dystrophy.

H Igarashi1, M Y Momoi, T Yamagata, H Shiraishi, I Eguchi.   

Abstract

Involvement of the cardiac conduction system is a common clinical feature in myotonic dystrophy, whereas the association of primary myocardial abnormalities has rarely been reported. A patient with a severe form of congenital myotonic dystrophy who developed fatal left ventricular hypertrophy at 3 months of age and died at 2 years of age is reported. Serial ultrasonographic studies revealed progressive left ventricular hypertrophy accompanied by outflow obstruction of the left ventricle. Southern analysis for the myotonin kinase gene revealed a 5.8 kb expansion of CTG repeats in addition to a fragment of normal length. The degree of expansion was much greater than those of other reported patients with congenital myotonic dystrophy. These findings suggest that left ventricular hypertrophy represents an extreme level of myocardial damage in myotonic dystrophy and that this damage may be related to the larger size of the CTG repeats.

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Year:  1998        PMID: 9588538     DOI: 10.1016/s0887-8994(97)00216-6

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  2 in total

1.  Transient complete atrioventricular block in a preterm neonate with congenital myotonic dystrophy: case report.

Authors:  Hee Na Kim; Young Kuk Cho; Joo Hyun Cho; Eun Mi Yang; Eun Song Song; Young Youn Choi
Journal:  J Korean Med Sci       Date:  2014-05-30       Impact factor: 2.153

2.  Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features.

Authors:  Warunee Dansithong; Cordula M Wolf; Partha Sarkar; Sharan Paul; Andy Chiang; Ian Holt; Glenn E Morris; Dorothy Branco; Megan C Sherwood; Lucio Comai; Charles I Berul; Sita Reddy
Journal:  PLoS One       Date:  2008-12-18       Impact factor: 3.240

  2 in total

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