Female patient with proximal myotonic myopathy and ventricular tachycardia

Zeitschrift fur Kardiologie

Volumn 94, Issue 11, 2005, Pages 754-760

  Schenk, S ^a   Loscher S ^a   Mickley, F ^a   Hartmann, A ^a  

^a Klinikum St Georg   (Germany)

Author keywords

Cardiomyopathy; Implantable defibrillator; Myotonic myopathy; Sudden cardiac death

Indexed keywords

AGED; ANAMNESIS; ARTICLE; ATRIOVENTRICULAR BLOCK; CARDIOMYOPATHY; CASE REPORT; DEFIBRILLATOR; ELECTROPHYSIOLOGY; FEMALE; HEART ATRIUM FLUTTER; HEART LEFT VENTRICLE FUNCTION; HEART VENTRICLE TACHYCARDIA; HUMAN; MYOTONIA;

AGED; DEFIBRILLATORS, IMPLANTABLE; FEMALE; HUMANS; MYOTONIC DISORDERS; TACHYCARDIA, VENTRICULAR;

EID: 27644489708     PISSN: 03005860     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00392-005-0281-7     Document Type: Article

References (26)

1. Andresen D (2004) Plötzlicher Herztod und Richtlinien zum plötzlichen Herztod. Z Kardiol 93(S1):i4-i6
2. Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard G, Thornton CA, Moxley RT, Harper PS, Rogers MR, Jurkat-Rott K, Lehmann-Horn F, Wieser T, Gamez J, Navarro C, Bottani A, Kohler A, Shriver MD, Sallinen R, Wessman M, Zhang S, Wright FA, Krahe R (2003) Confirmation of the type 2 myotonic dystrophy (CCTG) expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different european origins: a single shared haplotype indicates an ancestral founder effect. American Journal of Human Genetics 73:835-848
3. Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LPW (2003) Myotonic dystrophy type 2. Molecular, diagnostic and clinical spectrum. Neurology 60:657-664
4. Döhlemann C, Hebe J, Meitinger T et al (2000) Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the b-myosin heavy chain gene and cardiac arrest in childhood: a case report and family study. Z Kardiol 89(7):612-619
5. Eisenschenk S, Triggs WJ, Pearl GS, Rojiani AM (2001) Proximal myotonic myopathy: clinical, neuropathologic, and molecular genetic features. Annals of Clinical and Laboratory Science 31(2):140-146
6. Flachenecker P, Schneider C, Cursiefen S, Ricker K, Toyka KV, Reiners K (2003) Assesment of cardiovascular autonomic function in myotonic Dystrophy type 2 (DM2/PROMM). Neuromuscular Disorders 13:289-293
7. Held M, Schneider C, Fleischer K, Jany B (1988) Ein Patient mit Muskelschmerzen nach einer Tropenreise. Dtsch med Wochenschrift 123:1201-1206
8. Hofer JF, Wimmer G (2003) Severe heart failure from light chain cardiomyopathy (cardiac amyloidosis). Z Kardiol 92(1):90-95
9. Kohler A, Burkhard P, Hefft S, Bottani A, Pizzolato GP, Magistris MR (2000) Proximal myotonic myopathy: clinical, electrophysiological and pathological findings in a family. European Neurology 43:50-53
10. Malberg H, Bauernschmitt R, Meyerfeldt U et al (2003) Kurzzeit-Analyse der Herzfrequenzturbulenz versus Variabilitätsparameter und Barorezeptorsensitivität bei Patienten mit dilativer Kardiomyopathie. Z Kardiol 92(7):547-557
11. Mankodi A, Thornton CA (2002) Myotonic syndromes. Current Opinion in Neurology 15:545-552
12. Meola G (2002) Clinical and genetic heterogenity in myotonic dystrophies. Muscle Nerve 23:89-1799
13. Norman MW, McKenna WJ (1999) Arrhythmogenic right ventricular cardiomyopathy: Perspectives on disease. Z Kardiol 88(8):550-554
14. Peters S, Rust H, Trümmel M et al (2000) Familial hypertrophic cardiomyopathy associated with the prolongation of the QT interval. Z Kardiol 89(7):624-629
15. Phillips MF, Harper PS (1997) Cardiac disease in myotonic dystrophy. Cardiovascular Research 33:13-22
16. Ricker K, Koch MC, Lehmann-Horn F, Pongratz D, Speich N, Reiners K, Schneider C, Moxley RT (1995) Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy. Arch Neurol 52:25-31
17. Ricker K (1999) Myotonic dystrophy and proximal myotonic myopathy. J Neurol 246:334-338
18. Rudel R, Ruppersberg JP, Spittelmeister W (1989) Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodica. Muscle and Nerve 12:281-287
19. Schneider C, Reiners K, Toyka KV (2001) Myotone dystrophie (DM/Curschmann-Steinert-Erkrankung) und proximale myotone Myopathie (PROMM/Ricker-Syndrom). Myotone Erkrankungen mit multisystemischen Manifestationen. Nervenarzt 72:618-624
20. Schoser BGH, Schneider-Gold C, Kress W, Goebel HH, Reilich P, Koch MC, Pongratz DE, Toyka KV, Lochmüller H, Ricker K (2004) Muscle pathology in 57 patients with myotonic dystrophy type 2. Muscle and Nerve 29:275-281
21. Thornton A (1999) The myotonic dystrophies. Seminars in Neurology 19:25-33
22. Tokgozoglu LS, Ashiawa T, Pazifico A, Armstrong RM, Epstein HF, Zhoghbi WA (1995) Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assesment and relation to size of CTG repeat expansion. JAMA 274:813-819
23. von zur Mühlen F, Klass C, Kreuzer H, Mall G, Giese A, Reimers CD (1998) Cardiac involvement in proximal myotonic myopathy. Heart 79:619-621
24. Witzenbichler B, Schulze-Bahr E, Haverkamp W et al (2004) 18-jährige Patientin mit antiepileptischer Therapie und Kammerflimmern: Kasuistik eines hochmalignen LQT2-Syndroms. Z Kardiol 92(9):747-753
25. 54th ENMC International Workshop (1998) PROMM (Proximal Myotonic Myopathies) and other proximal myotonic syndromes. 12-12th October 1997, Narden, The Netherlands Neuromuscular Disorders 8:508-518
26. Annotation (1998) Proximal myotonic myopathie (PROMM) and other proximal myotonic syndromes. Neuromuscular Disorders 8:519-520