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Volumn 161, Issue 1, 2011, Pages 131-137

Patterns of cardiac and extracardiac anomalies in adults with tetralogy of Fallot

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANXIETY DISORDER; AORTA ARCH ANOMALY; AORTOPULMONARY FISTULA; ARTERY MALFORMATION; ARTICLE; ATTENTION DEFICIT DISORDER; CENTRAL NERVOUS SYSTEM MALFORMATION; CLINICAL FEATURE; COHORT ANALYSIS; CONTROLLED STUDY; DEPRESSION; EAR MALFORMATION; ENDOCRINE DISEASE; FACE DYSMORPHIA; FALLOT TETRALOGY; FEMALE; GASTROINTESTINAL MALFORMATION; GENE DELETION; GENETIC DISORDER; HEARING DISORDER; HEART ATRIUM SEPTUM DEFECT; HUMAN; HYPOCALCEMIA; HYPOTHYROIDISM; KARYOTYPE; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; MASS SCREENING; MUSCULOSKELETAL SYSTEM MALFORMATION; NEUROPSYCHIATRY; OTITIS MEDIA; PRIORITY JOURNAL; PROSPECTIVE STUDY; PULMONARY ARTERY; PULMONARY VALVE ATRESIA; PULMONARY VALVE DISEASE; RECURRENT DISEASE; SCHIZOPHRENIA; SCOLIOSIS; SEIZURE; SPEECH DISORDER; SUBCLAVIAN ARTERY; SUPERIOR CAVA VEIN; SYNDROME; THYROID DISEASE; UROGENITAL TRACT MALFORMATION; VEIN MALFORMATION;

EID: 78650268835     PISSN: 00028703     EISSN: 10976744     Source Type: Journal    
DOI: 10.1016/j.ahj.2010.09.015     Document Type: Article
Times cited : (26)

References (36)
  • 1
    • 0029029002 scopus 로고
    • Incidence of congenital heart disease: I. Postnatal incidence
    • Hoffman J.I. Incidence of congenital heart disease: I. Postnatal incidence Pediatr Cardiol 16 1995 103 113
    • (1995) Pediatr Cardiol , vol.16 , pp. 103-113
    • Hoffman, J.I.1
  • 5
    • 0035923555 scopus 로고    scopus 로고
    • NKX2.5 mutations in patients with tetralogy of fallot
    • Goldmuntz E., Geiger E., and Benson D.W. NKX2.5 mutations in patients with tetralogy of Fallot Circulation 104 2001 2565 2568 (Pubitemid 33104794)
    • (2001) Circulation , vol.104 , Issue.21 , pp. 2565-2568
    • Goldmuntz, E.1    Geiger, E.2    Benson, D.W.3
  • 8
    • 0024476864 scopus 로고
    • Congential cardiovascular malformations associated with chromosome abnormalities: An epidemiologic study
    • DOI 10.1016/S0022-3476(89)80605-5
    • Ferencz C., Neill C.A., and Boughman J.A. Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study J Pediatr 114 1989 79 86 (Pubitemid 19027744)
    • (1989) Journal of Pediatrics , vol.114 , Issue.1 , pp. 79-86
    • Ferencz, C.1    Neill, C.A.2    Boughman, J.A.3    Rubin, J.D.4    Brenner, J.I.5    Perry, L.W.6
  • 9
    • 0023113595 scopus 로고
    • Spectrum of congenital heart disease in CHARGE association
    • DOI 10.1016/S0022-3476(87)80555-3
    • Cyran S.E., Martinez R., and Daniels S. Spectrum of congenital heart disease in CHARGE association J Pediatr 110 1987 576 578 (Pubitemid 17049049)
    • (1987) Journal of Pediatrics , vol.110 , Issue.4 , pp. 576-578
    • Cyran, S.E.1    Martinez, R.2    Daniels, S.3
  • 10
    • 56349136292 scopus 로고    scopus 로고
    • Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease
    • Fung W.L., Chow E.W., and Webb G.D. Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease Int J Cardiol 131 2008 51 58
    • (2008) Int J Cardiol , vol.131 , pp. 51-58
    • Fung, W.L.1    Chow, E.W.2    Webb, G.D.3
  • 12
    • 58149446009 scopus 로고
    • Congenital anomalies in the newborn infant, including minor variations. A study of 4,412 babies by surface examination for anomalies and buccal smear for sex chromatin
    • Marden P.M., Smith D.W., and McDonald M.J. Congenital anomalies in the newborn infant, including minor variations. A study of 4,412 babies by surface examination for anomalies and buccal smear for sex chromatin J Pediatr 64 1964 357 371
    • (1964) J Pediatr , vol.64 , pp. 357-371
    • Marden, P.M.1    Smith, D.W.2    McDonald, M.J.3
  • 15
    • 57549106250 scopus 로고    scopus 로고
    • Late risk of outcomes for adults with repaired tetralogy of Fallot from an inception cohort spanning four decades
    • Hickey E.J., Veldtman G., and Bradley T.J. Late risk of outcomes for adults with repaired tetralogy of Fallot from an inception cohort spanning four decades Eur J Cardiothorac Surg 35 2009 156 164
    • (2009) Eur J Cardiothorac Surg , vol.35 , pp. 156-164
    • Hickey, E.J.1    Veldtman, G.2    Bradley, T.J.3
  • 16
    • 0031920989 scopus 로고    scopus 로고
    • Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of fallot and pulmonary atresia-ventricular septal defect
    • Chessa M., Butera G., and Bonhoeffer P. Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect Heart 79 1998 186 190 (Pubitemid 28157341)
    • (1998) Heart , vol.79 , Issue.2 , pp. 186-190
    • Chessa, M.1    Butera, G.2    Bonhoeffer, P.3    Iserin, L.4    Kachaner, J.5    Lyonnet, S.6    Munnich, A.7    Sidi, D.8    Bonnet, D.9
  • 17
    • 0029143637 scopus 로고
    • Non-cardiac malformations in individuals with outflow tract defects of the heart: The Baltimore-Washington Infant Study (1981-1989)
    • Lurie I.W., Kappetein A.P., and Loffredo C.A. Non-cardiac malformations in individuals with outflow tract defects of the heart: the Baltimore-Washington Infant Study (1981-1989) Am J Med Genet 59 1995 76 84
    • (1995) Am J Med Genet , vol.59 , pp. 76-84
    • Lurie, I.W.1    Kappetein, A.P.2    Loffredo, C.A.3
  • 19
    • 66249105352 scopus 로고    scopus 로고
    • Extracardiac lesions and chromosomal abnormalities associated with major fetal heart defects: Comparison of intrauterine, postnatal and postmortem diagnoses
    • Song M.S., Hu A., and Dyhamenahali U. Extracardiac lesions and chromosomal abnormalities associated with major fetal heart defects: comparison of intrauterine, postnatal and postmortem diagnoses Ultrasound Obstet Gynecol 33 2009 552 559
    • (2009) Ultrasound Obstet Gynecol , vol.33 , pp. 552-559
    • Song, M.S.1    Hu, A.2    Dyhamenahali, U.3
  • 20
    • 75549124539 scopus 로고
    • Extracardiac congenital malformations in Children with congenital heart diseases
    • Boesen I., Melchior J.C., and Terslev E. Extracardiac congenital malformations in Children with congenital heart diseases Acta Paediatr Suppl 146 1963 28 33
    • (1963) Acta Paediatr Suppl , vol.146 , pp. 28-33
    • Boesen, I.1    Melchior, J.C.2    Terslev, E.3
  • 21
    • 0032955014 scopus 로고    scopus 로고
    • Prevalence of congenital malformations and genetic diseases in Korea
    • Jung S.C., Kim S.S., and Yoon K.S. Prevalence of congenital malformations and genetic diseases in Korea J Hum Genet 44 1999 30 34
    • (1999) J Hum Genet , vol.44 , pp. 30-34
    • Jung, S.C.1    Kim, S.S.2    Yoon, K.S.3
  • 26
    • 0023212370 scopus 로고
    • Thyrocalcitonin-containing cells in the Di George anomaly
    • DOI 10.1016/S0046-8177(87)80165-X
    • Burke B.A., Johnson D., and Gilbert E.F. Thyrocalcitonin-containing cells in the Di George anomaly Hum Pathol 18 1987 355 360 (Pubitemid 17071033)
    • (1987) Human Pathology , vol.18 , Issue.4 , pp. 355-360
    • Burke, B.A.1    Johnson, D.2    Gilbert, E.F.3
  • 27
    • 0028579773 scopus 로고
    • Autoimmune thyroid disease: Further developments in our understanding
    • Weetman A.P., and McGregor A.M. Autoimmune thyroid disease: further developments in our understanding Endocr Rev 15 1994 788 830
    • (1994) Endocr Rev , vol.15 , pp. 788-830
    • Weetman, A.P.1    McGregor, A.M.2
  • 28
    • 37549061731 scopus 로고    scopus 로고
    • Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of Fallot
    • Zeltser I., Jarvik G.P., and Bernbaum J. Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of Fallot J Thorac Cardiovasc Surg 135 2008 91 97
    • (2008) J Thorac Cardiovasc Surg , vol.135 , pp. 91-97
    • Zeltser, I.1    Jarvik, G.P.2    Bernbaum, J.3
  • 30
    • 77955379566 scopus 로고    scopus 로고
    • Copy number variations in schizophrenia: Critical review and new perspectives on concepts of genetics and disease
    • Bassett A.S., Scherer S.W., and Brzustowicz L.M. Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease Am J Psychiatry 167 2010 899 914
    • (2010) Am J Psychiatry , vol.167 , pp. 899-914
    • Bassett, A.S.1    Scherer, S.W.2    Brzustowicz, L.M.3
  • 31
    • 68149181705 scopus 로고    scopus 로고
    • De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
    • Greenway S.C., Pereira A.C., and Lin J.C. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot Nat Genet 41 2009 931 935
    • (2009) Nat Genet , vol.41 , pp. 931-935
    • Greenway, S.C.1    Pereira, A.C.2    Lin, J.C.3
  • 32
    • 78650276262 scopus 로고    scopus 로고
    • 13q13.1-q13.2 deletion in tetralogy of Fallot: Clinical report and a literature review
    • 10.1016/j.ijcard.2010.05.070 (e-published)
    • Costain G., Silversides C.K., and Marshall C.R. 13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review Int J Cardiol 2010 10.1016/j.ijcard.2010.05.070 (e-published)
    • (2010) Int J Cardiol
    • Costain, G.1    Silversides, C.K.2    Marshall, C.R.3
  • 34
    • 56049097929 scopus 로고    scopus 로고
    • High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease
    • Erdogan F., Larsen L.A., and Zhang L. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease J Med Genet 45 2008 704 709
    • (2008) J Med Genet , vol.45 , pp. 704-709
    • Erdogan, F.1    Larsen, L.A.2    Zhang, L.3
  • 35
    • 0016680481 scopus 로고
    • Extracardiac abnormalities in infants with congenital heart disease
    • Greenwood R.D., Rosenthal A., and Parisi L. Extracardiac abnormalities in infants with congenital heart disease Pediatrics 55 1975 485 492
    • (1975) Pediatrics , vol.55 , pp. 485-492
    • Greenwood, R.D.1    Rosenthal, A.2    Parisi, L.3
  • 36
    • 77952032690 scopus 로고    scopus 로고
    • Consensus statement: Chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
    • Miller D.T., Adam M.P., and Aradhya S. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies Am J Hum Genet 86 2010 749 764
    • (2010) Am J Hum Genet , vol.86 , pp. 749-764
    • Miller, D.T.1    Adam, M.P.2    Aradhya, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.