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Volumn 152, Issue 1, 2010, Pages 191-195

Left ventricular noncompaction: A rare disorder in adults and its association with 1p36 chromosomal anomaly

Author keywords

2D TTE (two dimensional transthoracic echocardiography); Deletion 1p36; Left ventricular noncompaction; Unclassified cardiomyopathy

Indexed keywords

CARVEDILOL; ECHO CONTRAST MEDIUM; ETIRACETAM; FUROSEMIDE; PHENOBARBITAL; SPIRONOLACTONE;

EID: 75149196314     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33155     Document Type: Article
Times cited : (5)

References (27)
  • 3
    • 0025106446 scopus 로고
    • Isolated noncompaction of left ventricular myocardium: A study of eight cases
    • Chin TK, Perloff JK, Williams RG, Jue K, Mohrmann R. 1990. Isolated noncompaction of left ventricular myocardium: A study of eight cases. Circulation 82:507-513.
    • (1990) Circulation , vol.82 , pp. 507-513
    • Chin, T.K.1    Perloff, J.K.2    Williams, R.G.3    Jue, K.4    Mohrmann, R.5
  • 4
    • 56649091290 scopus 로고    scopus 로고
    • Left-ventricular no-ncompaction (LVNC): A clinical feature more often observed in terminal deletion 1p36 than previously expected
    • Cremer K, Ludecke H, Ruhr F, Wleczorek D. 2008. Left-ventricular no-ncompaction (LVNC): A clinical feature more often observed in terminal deletion 1p36 than previously expected. Eur J Med Genet 51:685-688.
    • (2008) Eur J Med Genet , vol.51 , pp. 685-688
    • Cremer, K.1    Ludecke, H.2    Ruhr, F.3    Wleczorek, D.4
  • 6
    • 0141955800 scopus 로고    scopus 로고
    • Population data suggest that deletion of 1p36 are a relatively common chromosome abnormality
    • Heilstedt HA, Ballif BC, Howard LA, Kashork CD, Shaffer LG. 2003. Population data suggest that deletion of 1p36 are a relatively common chromosome abnormality. Clin Genet 64:310-316.
    • (2003) Clin Genet , vol.64 , pp. 310-316
    • Heilstedt, H.A.1    Ballif, B.C.2    Howard, L.A.3    Kashork, C.D.4    Shaffer, L.G.5
  • 10
    • 0022446677 scopus 로고
    • Persisting myocardial sinusoids of both ventricles as an isolated anomaly: Echocardiographic, angiographic, and pathologic anatomical findings
    • Jenni R, Goebel N, Tartini R, Schneider J, Arbenz U, Oelz O. 1986. Persisting myocardial sinusoids of both ventricles as an isolated anomaly: Echocardiographic, angiographic, and pathologic anatomical findings. Cardiovasc Intervent Radiol 9:127-131.
    • (1986) Cardiovasc Intervent Radiol , vol.9 , pp. 127-131
    • Jenni, R.1    Goebel, N.2    Tartini, R.3    Schneider, J.4    Arbenz, U.5    Oelz, O.6
  • 15
    • 0033853552 scopus 로고    scopus 로고
    • Long-term follow-up of 34 adults with isolated left ventricular non-compaction: A distinct cardiomyopathy with poor prognosis
    • Oechslin EN, Attenhofer Jost CH, Rojas JR, Kaufmann PA, Jenni R. 2000. Long-term follow-up of 34 adults with isolated left ventricular non-compaction: A distinct cardiomyopathy with poor prognosis. J Am Coll Cardiol 36:493-500.
    • (2000) J Am Coll Cardiol , vol.36 , pp. 493-500
    • Oechslin, E.N.1    Attenhofer Jost, C.H.2    Rojas, J.R.3    Kaufmann, P.A.4    Jenni, R.5
  • 16
    • 0032076955 scopus 로고    scopus 로고
    • Actin mutations in dilated cardiomyopathy: A heritable form of heart failure
    • Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT. 1998. Actin mutations in dilated cardiomyopathy: A heritable form of heart failure. Science 280:750-752.
    • (1998) Science , vol.280 , pp. 750-752
    • Olson, T.M.1    Michels, V.V.2    Thibodeau, S.N.3    Tai, Y.S.4    Keating, M.T.5
  • 18
    • 56049116986 scopus 로고    scopus 로고
    • Bilateral perisylvian polymicrogyria, periventricular nodular heterotopias, and left ventricular noncompaction in a girl with 10.5-11.1Mb terminal deletion of 1p36
    • Saito S, Kawamura R, Kosho T, Shimizu T, Aoyama K, Koike K, Matsumoto N, Kato M, Wakui K, Fukushima Y. 2008. Bilateral perisylvian polymicrogyria, periventricular nodular heterotopias, and left ventricular noncompaction in a girl with 10.5-11.1Mb terminal deletion of 1p36. Am J Med Genet Part A 146A:2891-2897.
    • (2008) Am J Med Genet , vol.146 A , Issue.PART A , pp. 2891-2897
    • Saito, S.1    Kawamura, R.2    Kosho, T.3    Shimizu, T.4    Aoyama, K.5    Koike, K.6    Matsumoto, N.7    Kato, M.8    Wakui, K.9    Fukushima, Y.10
  • 19
    • 0041821469 scopus 로고    scopus 로고
    • Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients
    • Sasse-Klaassen S, Gerull B, Oechslin E, Jenni R, Thierfelder L. 2003. Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients. Am J Med Genet Part A 119A:162-167.
    • (2003) Am J Med Genet , vol.119 A , Issue.PART A , pp. 162-167
    • Sasse-Klaassen, S.1    Gerull, B.2    Oechslin, E.3    Jenni, R.4    Thierfelder, L.5
  • 21
    • 0030194396 scopus 로고    scopus 로고
    • Trabeculation in the human heart
    • Sedmera D, Thomas PS. 1996. Trabeculation in the human heart. Bioessays 18:607.
    • (1996) Bioessays , vol.18 , pp. 607
    • Sedmera, D.1    Thomas, P.S.2
  • 24
    • 0021369911 scopus 로고
    • The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with a 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1
    • Steele MW, Wegner SL, Geweke LO, Golden WL. 1984. The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with a 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1. Clin Genet 25:59-562.
    • (1984) Clin Genet , vol.25 , pp. 59-562
    • Steele, M.W.1    Wegner, S.L.2    Geweke, L.O.3    Golden, W.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.