• 1
    Chin TK, Perlof JK, Williams RG, Jue K, Mohrmann R. Isolated noncompaction of left ventricular myocardium: a study of eight cases. Circulation 1990: 82: 507513.
  • 2
    Finsterer J. Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction. Pediatr Cardiol 2009: 30: 659681.
  • 3
    Ichida F, Tsubata S, Bowles KR et al. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. Circulation 2001: 103: 12561263.
  • 4
    Pignatelli RH, McMahon CJ, Dreyer WJ et al. Clinical characterization of left ventricular noncompaction in children. A relatively common form of cardiomyopathy. Circulation 2003: 108: 26722678.
  • 5
    Cremer K, Ruhr F, Wieczorek D. Left-ventricular non-compaction (LVNC): a clinical feature more often observed in terminal deletion 1p36 than previously expected. Eur J Med Genet 2008: 51: 685688.
  • 6
    Kanemoto N, Horigome H, Nakayama J et al. Interstitial 1q43-q43 deletion with left ventricular noncompaction myocardium. Eur J Med Genet 2006: 49: 247253.
  • 7
    Pauli RM, Scheib-Wixted S, Cripe L, Izumo S, Sekhon GS. Ventricular noncompaction and distal 5q deletion. Am J Med Genet 1999: 85: 419423.
  • 8
    Blinder JJ, Martinez HR, Craigen WJ, Belmont J, Pignatelli RH, Jefferies JL. Noncompaction of the left ventricular myocardium in a boy with a novel chromosome 8p23.1 deletion. Am J Med Genet 2011: 155: 22152220.
  • 9
    McMahon CJ, Chang AC, Pignatelli RH et al. Left ventricular noncompaction cardiomyopathy in association with trisomy 13. Pediatr Cardiol 2005: 26: 477479.
  • 10
    Beken S, Cevik A, Turan O et al. A neonatal case of left ventricular noncompaction associated with trisomy 18. Genet Couns 2011: 22: 161164.
  • 11
    Madan S, Madan-Khetarpal S, Park SC et al. Left ventricular non-compaction on MRI in a patient with 22q11.2 distal deletion. Am J Med Genet 2010: 152A: 12951299.
  • 12
    van Heerde M, Hruda J, Azekamp MG. Severe pulmonary hypertension secondary to a parachute-like mitral valve, with the left superior caval vein draining into the coronary sinus, in a girl with Turner's syndrome. Cardiol Young 2003: 13: 364366.
  • 13
    Bleyl SB, Mumford BR, Thompson V et al. Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome. Am J Hum Genet 1997: 61: 868872.
  • 14
    Budde BS, Binner P, Waldmuller S et al. Noncompaction of the ventricular myocardium is associated with a de novo mutation in the Beta-Myosin Heavy Chain gene. PLoS One 2007: 2: e1362.
  • 15
    Jenni R, Oechslin E, Schneider J et al. Echocardiographic and pathoanatomical characteristics of isolated noncompaction: a step towards classification as a distinct cardiomyopahy. Heart 2001: 86: 666671.
  • 16
    Bernardini L, Castori M, Capalbo A et al. Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplication. Am J Med Genet 2007: 143A: 29372943.
  • 17
    Branton H, Warren AE, Penney LS. Left ventricular noncompaction and coronary artery fistula in an infant with deletion 22q11.2. Pediatr Cardiol 2011: 32: 208210.
  • 18
    Altenberger H, Stöllberger C, Finsterer J. Isolated left ventricular hypertrabeculation/noncompaction in a Turner mosaic with male phenotype. Acta Cardiol 2009: 64: 99103.
  • 19
    Battaglia A, Hoyme HE, Dallapiccola B et al. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation. Pediatrics 2008: 121: 404410.
  • 20
    Thienpont B, Mertens L, Buyse G et al. Left-ventricular noncompaction in a patient with monosomy 1p36. Eur J Med Genet 2007: 50: 233236.
  • 21
    Pearce FB, Litovsky SH, Dabal RJ et al. Pathologic features of dilated cardiomyopathy with localized noncompaction in a child with deletion 1p36 syndrome. Congenit Heart Dis 2012: 7: 5961.
  • 22
    Kwiatkowski D, Hagenbuch S, Meyer R. A teenager with Marfan syndrome and left ventricular noncompaction. Pediatr Cardiol 2010: 31: 132135.
  • 23
    Amman G, Sherman FS. Myocardial dysgenesis with persistent sinusoids in a neonate with Noonan's phenotype. Pediatr Pathol 1992: 12: 8392.
  • 24
    Limongelli G, Pacileo G, Marino B et al. Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome. Am J Cardiol 2007: 100: 736741.
  • 25
    Fazio G, Pipitone S, Iacona MA et al. The noncompaction of the left ventricular myocardium: our paediatric experience. J Cardiovasc Med 2007: 8: 904908.