Familial left ventricular hypertrabeculation in myotonic dystrophy type 1

Herz

Volumn 28, Issue 5, 2003, Pages 466-470

  Finsterer, Josef ^a   Stöllberger, Claudia ^b   Kopsa, Wolfgang ^c  

^a Department of Neurology ^*  (Austria)

^b 2nd Medical Department   (Austria)

^c KRANKENANSTALT RUDOLFSTIFTUNG   (Austria)

Author keywords

Cardiac involvement; Cardiac MRI; Cardiomyopathy; ECG abnormalities; Echocardiography; Genetics; Hereditary; Muscular dystrophy; Myotonia; Neuromuscular disorder; Non compaction

Indexed keywords

CREATINE KINASE; PROTEIN KINASE;

ADOLESCENT; ADULT; ARTICLE; CARDIOMYOPATHY; CARDIOVERSION; CASE REPORT; CHROMOSOME 19; CREATINE KINASE BLOOD LEVEL; DMPK GENE; DNA DETERMINATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; FAMILIAL DISEASE; FEMALE; GENE; HEART ATRIUM FLUTTER; HETEROZYGOSITY; HETEROZYGOTE; HUMAN; LEFT VENTRICULAR HYPERTRABECULATION; MALE; MUSCLE ATROPHY; MUSCLE CRAMP; MUSCLE WEAKNESS; MYOTONIC DYSTROPHY; NUCLEOTIDE REPEAT; PHENOTYPE; SINUS RHYTHM; ST SEGMENT ELEVATION; TRANSTHORACIC ECHOCARDIOGRAPHY;

ADOLESCENT; CARDIOMYOPATHIES; CHROMOSOMES, HUMAN, PAIR 19; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; HEART VENTRICLES; HETEROZYGOTE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MYOTONIC DYSTROPHY; PHENOTYPE; PROTEIN KINASES;

EID: 0042425956     PISSN: 03409937     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00059-003-2437-4     Document Type: Article

References (31)

1. Bleyl SB, Mumford BR, Brown-Harrison M-C, Pagotto LC, Carey JC, Pysher TJ, Ward K, Chin TK. Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals. Am J Med Genet 1997;72:257-65.
2. Chin TK, Perloff JK, Williams RG, Joe K, Muhrmann R. Isolated noncompaction of the left ventricular myocardium. A study of eight cases. Circulation 1990;82:507-13.
3. Finsterer J, Stöllberger C, Kopsa W, Jaksch M. Wolff-Parkinson-White syndrome and isolated left ventricular abnormal trabeculation as a manifestation of Leber's hereditary optic neuropathy. Can J Cardiol 2001;17:464-6.
4. Stöllberger C, Finsterer J, Blazek G. Left ventricular hypertrabeculation/non-compaction and association with additional cardiac and neuromuscular disorders. Am J Cardiol 2002;90:899-902.
5. Stöllberger C, Finsterer J, Blazek G. Isolated left ventricular abnormal trabeculation: follow-up and association with neuromuscular disorders. Can J Cardiol 2001;17:163-8.
6. Finsterer J, Stöllberger C, Jarius C, Wegmann R, Janssen B. Left ventricular hypertrabeculation in myotonic dystrophy type 1. Herz 2001;26:287-90.
7. Digilio MC, Marino B, Bevilacqua M, Musolino AM, Giannotti A, Dallapiccola B. Genetic heterogeneity of isolated noncompaction of the left ventricular myocardium. Am J Med Genet 1999;85: 90-1.
8. Finsterer J, Stöllberger C, Michaela J. Familial left ventricular hypertrabeculation in two blind brothers. Cardiovasc Pathol 2002; 11:146-8.
9. Hamamichi Y, Ichida F, Hashimoto I, Uese KH, Miyawaki T, Tsukano S, Ono Y, Echigo S, Kamiya T. Isolated noncompaction of the ventricular myocardium: ultrafast computed tomography and magnetic resonance imaging. Int J Card Imaging 2001;17:305-14.
10. Ichida F, Hamamichi Y, Miyawaki T, et al. Clinical features of isolated noncompaction of the ventricular myocardium. Long-term clinical course, hemodynamic properties, and genetic background. J Am Coll Cardiol 1999;34:233-40.
11. Kurosaki K, Ikeda U, Hojo Y, Fujikawa H, Katsuki T, Shimada K. Familial isolated noncompaction of the left ventricular myocardium. Cardiology 1999;91:69-72.
12. Matsuda M, Tsukahara M, Kondoh O, Mito H. Familial isolated noncompaction of ventricular myocardium. J Hum Genet 1999; 44:126-8.
13. Ritter M, Oechslin E, Sütsch G, Attenhofer C, Schneider J, Jenni R. Isolated noncompaction of the myocardium in adults. Mayo Clin Proc 1997;72:26-31.
14. Harper PS, Rüdel R. Myotonic dystrophy. In: Engel AG, Franzini-Armstrong C, eds. Myology, Basic and clinics. New York: McGraw-Hill, 1994:1192-219.
15. Gharehbaghi-Schnell E, Finsterer J, Korschineck I, Mamoli B, Binder BR. Genotype-phenotype correlation in myotonic dystrophy. Clin Genet 1998;53:20-6.
16. Finsterer J, Gharehbaghi-Schnell E, Korschineck L, Fheodoroff K, Seiser A, Löscher W, Binder BR, Mamoli B. Phenotype and CTG-repeat size in myotonic dystrophy: a study of 26 patients and 55 relatives. J Neurogenet 1999;13:181-90.
17. Finsterer J. Myotonic dystrophy type 2. Eur J Neurol 2002;9:441-7.
18. Finsterer J, Stöllberger C, Köcher K, Mamoli B. ECG abnormalities in myopathies, coronary heart disease and controls. Herz 1997; 22:277-82.
19. Finsterer J, Stöllberger C, Keller H, Slany J, Mamoli B. Cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy. Herz 1997;22:96-103.
20. Finsterer J, Stöllberger C, Blazek G, Spahits E. Cardiac involvement in myotonic dystrophy, Becker muscular dystrophy and mitochondrial myopathy: a five-year follow-up. Can J Cardiol 2001;17:1061-9.
21. Nguyen HH, Wolfe JT, Holmes DR, Edwards WD. Pathology of the cardiac conduction system in myotonic dystrophy: a study of 17 cases. J Am Coll Cardiol 1988;11:662-71.
22. Igarashi H, Momoi MY, Yamagata T, Shiraishi H, Eguchi I. Hypertrophic cardiomyopathy in congenital myotonic dystrophy. Pediatr Neurol 1998;18:366-9.
23. Nakada T, Yonesaka S. "Hypertrophic cardiomyopathy" in a girl with adult-type myotonic dystrophy. Pediatr Int 1999;41:586-8.
24. Wake M, Matsushita M, Aono H, Matsumoto M, Kohri Y. Perioperative management of a patient with myotonic dystrophy developing the cardiac symptoms initially prior to the neuromuscular symptoms. Masui 1994;43:1238-42.
25. Sonaglioni G, Curatola L, Bollettini G, Agostini L, Franchetta G, Pa N, Pignotti M, Floris B. Echocardiographic findings in dystrophia myotonica. G Ital Cardiol 1984;14:551-6.
26. Finsterer J, Gharehbaghi-Schnell E, Stöllberger C, Fheodoroff A, Seiser A. Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy. Clin Genet 2001;59:350-5.
27. Finsterer J, Stöllberger C. Spontaneous left ventricular hypertrabeculation in dystrophin duplication based Becker muscular dystrophy. Herz 2001;26:477-81.
28. Daimon Y, Watanabe S, Takeda S, Hijikata Y, Komuro I. Two-layered appearance of noncompaction of the ventricular myocardium on magnetic resonance imaging. Circ J 2002;66:619-21.
29. Borreguero LJ, Corti R, deSoria RF, Osende JI, Fuster V, Badimon JJ. Images in cardiovascular medicine. Diagnosis of isolated noncompaction of the myocardium by magnetic resonance imaging. Circulation 2002;105:E177-8.
30. Dagdeviren B, Eren M, Oguz E. Noncompaction of ventricular myocardium, complete atrioventricular block and minor congenital heart abnormalities: case report of an unusual coexistence. Acta Cardiol 2002;57:221-4.
31. Valdes-Daepena M, Gilbert-Barness E. Cardiovascular causes of sudden infant death. Pediatr Pathol Mol Med 2002;21:195-211.