Intrafamilial variability of noncompaction of the ventricular myocardium

American Heart Journal

Volumn 151, Issue 5, 2006, Pages 1012.e7-1012.e14

  Johnson, Mark T ^a   Zhang, Shaoxiong ^b   Gilkeson, Robert ^b   Ameduri, Rebecca ^b   Chebotarev, Oleg ^b   Kenton, Alexander B ^c   Bowles, Karla R ^c   Towbin, Jeffrey A ^c   Robin, Nathaniel H ^d   Brozovich, Frank ^b   Hoit, Brian D ^b  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROBREVIN;

ADOLESCENT; ADULT; AGED; ARTICLE; CARDIOMYOPATHY; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC TEST; DIAGNOSTIC VALUE; DISEASE SEVERITY; EVALUATION; FAMILY; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENETIC VARIABILITY; HEART VENTRICLE FUNCTION; HUMAN; INFANT; MALE; NONCOMPACTION OF VENTRICULAR MYOCARDIUM; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; TWO DIMENSIONAL ECHOCARDIOGRAPHY; ECHOCARDIOGRAPHY; ECHOGRAPHY; ELECTROCARDIOGRAPHY; GENETICS; HEART VENTRICLE; MIDDLE AGED; NEWBORN; PATHOPHYSIOLOGY; PEDIGREE; PHENOTYPE; PRENATAL DEVELOPMENT;

ADOLESCENT; CARDIOMYOPATHIES; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; HEART VENTRICLES; HUMANS; INFANT; INFANT, NEWBORN; MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; ULTRASONOGRAPHY, PRENATAL; VARIATION (GENETICS); VENTRICULAR DYSFUNCTION;

EID: 33646083216     PISSN: 00028703     EISSN: 10976744     Source Type: Journal    
DOI: 10.1016/j.ahj.2006.01.021     Document Type: Article

References (18)

1. Towbin J.A., and Bowles N.E. The failing heart. Nature 415 (2002) 227-233
2. Jenni R., Oechslin E., Schneider J., et al. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy. Heart 86 (2001) 666-671
3. Stollberger C., Finsterer J., Valentin A., et al. Isolated left ventricular abnormal trabeculation in adults is associated with neuromuscular disorders. Clin Cardiol 22 (1999) 119-123
4. Chen R., Tsuji T., Ichida F., et al. Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction. Mol Genet Metab 77 (2002) 319-325
5. Ichida F., Tsubata S., Bowles K.R., et al. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. Circulation 103 (2001) 1256-1263
6. Vatta M., Mohapatra B., Jimenez S., et al. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J Am Coll Cardiol 42 (2003) 2014-2027
7. Hermida-Prieto M., Monserrat L., Castro-Beiras A., et al. Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. Am J Cardiol 94 (2004) 50-54
8. Kenton A.B., Sanchez X., Coveler K.J., et al. Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK binding protein-12. Mol Genet Metab 82 (2004) 162-166
9. Sasse-Klaassen S., Probst S., Gerull B., et al. Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15. Circulation 109 (2004) 2720-2723
10. Chung T., Yiannikas J., Lee L.C., et al. Isolated noncompaction involving the left ventricular apex in adults. Am J Cardiol 94 (2004) 1214-1216
11. Bowles K.R., Abraham S.E., Brugada R., et al. Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes. Genomics 67 (2000) 109-127
12. Pignatelli R.H., McMahon C.J., Dreyer W.J., et al. Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy. Circulation 108 (2003) 2672-2678
13. Ellis C., Pymar H., Windrim R., et al. A puzzling intrauterine death: non-compaction of the fetal ventricular myocardium presenting with reversed end-diastolic flow velocity in the umbilical arteries. J Obstet Gynaecol Can 27 (2005) 695-698
14. Moura C., Hillion Y., Daikha-Dahmane F., et al. Isolated non-compaction of the myocardium diagnosed in the fetus: two sporadic and two familial cases. Cardiol Young 12 (2002) 278-283
15. 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 34 (1999) 233-240
16. Soler R., Rodriguez E., Monserrat L., et al. MRI of subendocardial perfusion deficits in isolated left ventricular noncompaction. J Comput Assist Tomogr 26 (2002) 373-375
17. Borges A.C., Kivelitz D., and Baumann G. Isolated left ventricular non-compaction: cardiomyopathy with homogeneous transmural and heterogeneous segmental perfusion. Heart 89 (2003) e21
18. Korcyk D., Edwards C.C., Armstrong G., et al. Contrast-enhanced cardiac magnetic resonance in a patient with familial isolated ventricular non-compaction. J Cardiovasc Magn Reson 6 (2004) 569-576