메뉴 건너뛰기




Volumn 166, Issue 2, 2007, Pages 111-116

Familial recurrence of congenital heart disease: An overview and review of the literature

Author keywords

Familial recurrence of congenital heart disease

Indexed keywords

CONGENITAL HEART DISEASE; FALLOT TETRALOGY; GREAT VESSELS TRANSPOSITION; HEART ATRIUM SEPTUM DEFECT; HEART DISEASE; HEART LEFT RIGHT SHUNT; HUMAN; INHERITANCE; PRIORITY JOURNAL; RECURRENT DISEASE; REVIEW; RISK;

EID: 33845913514     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-006-0295-9     Document Type: Review
Times cited : (68)

References (50)
  • 7
    • 0028060395 scopus 로고
    • Familial atrioventricular septal defect: Possible genetic mechanism
    • Digilio MC, Marino B, Giannotti A, Dallapiccola B (1994) Familial atrioventricular septal defect: possible genetic mechanism. Br Heart J 72:301
    • (1994) Br Heart J , vol.72 , pp. 301
    • Digilio, M.C.1    Marino, B.2    Giannotti, A.3    Dallapiccola, B.4
  • 9
    • 0031037933 scopus 로고    scopus 로고
    • Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion
    • Digilio MC, Marino B, Giannotti A, Toscano A, Dallapiccola B (1997) Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion. J Med Genet 34:188-190
    • (1997) J Med Genet , vol.34 , pp. 188-190
    • Digilio, M.C.1    Marino, B.2    Giannotti, A.3    Toscano, A.4    Dallapiccola, B.5
  • 16
    • 0020640744 scopus 로고
    • Evidence of congenital heart disease in the offspring of parents with atrioventricular defects
    • Emanuel R, Somerville J, Inns A, Withers R (1983) Evidence of congenital heart disease in the offspring of parents with atrioventricular defects. Br Heart J 49:144-147
    • (1983) Br Heart J , vol.49 , pp. 144-147
    • Emanuel, R.1    Somerville, J.2    Inns, A.3    Withers, R.4
  • 18
    • 0014370616 scopus 로고
    • A family study in transposition of the great vessels and in tricuspid atresia
    • Fuhrmann W (1968) A family study in transposition of the great vessels and in tricuspid atresia. Humangenetik 6:148-157
    • (1968) Humangenetik , vol.6 , pp. 148-157
    • Fuhrmann, W.1
  • 21
    • 0027959394 scopus 로고
    • Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal
    • Gennarelli M, Novelli G, Digilio MC, Giannotti A, Marino B, Dallapiccola B (1994) Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal. Hum Genet 94:708-710
    • (1994) Hum Genet , vol.94 , pp. 708-710
    • Gennarelli, M.1    Novelli, G.2    Digilio, M.C.3    Giannotti, A.4    Marino, B.5    Dallapiccola, B.6
  • 22
    • 0035923555 scopus 로고    scopus 로고
    • NKX2.5 mutations in patients with tetralogy of Fallot
    • Goldmuntz E, Geiger E, Benson DW (2001) NKX2.5 mutations in patients with tetralogy of Fallot. Circulation 104:2565-2568
    • (2001) Circulation , vol.104 , pp. 2565-2568
    • Goldmuntz, E.1    Geiger, E.2    Benson, D.W.3
  • 23
    • 0028566793 scopus 로고
    • Possible genes for left heart formation on 11q23.3
    • Guenthard J, Buehler E, Jaeggi E, Wyler F (1994) Possible genes for left heart formation on 11q23.3. Ann Genet 37:143-146
    • (1994) Ann Genet , vol.37 , pp. 143-146
    • Guenthard, J.1    Buehler, E.2    Jaeggi, E.3    Wyler, F.4
  • 24
    • 0028177860 scopus 로고
    • Familial atrioventricular septal defect: Possible genetic mechanisms
    • Kumar A, Williams CA, Victorica BE (1994) Familial atrioventricular septal defect: possible genetic mechanisms. Br Heart J 71:79-81
    • (1994) Br Heart J , vol.71 , pp. 79-81
    • Kumar, A.1    Williams, C.A.2    Victorica, B.E.3
  • 25
    • 0346492855 scopus 로고    scopus 로고
    • Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries
    • Loffredo CA, Chokkalingam A, Sill AM, Boughman JA, Clark EB, Scheel J, Brenner JI (2004) Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries. Am J Med Genet A 124:225-230
    • (2004) Am J Med Genet A , vol.124 , pp. 225-230
    • Loffredo, C.A.1    Chokkalingam, A.2    Sill, A.M.3    Boughman, J.A.4    Clark, E.B.5    Scheel, J.6    Brenner, J.I.7
  • 26
    • 0025004644 scopus 로고
    • Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome
    • Marino B, Vairo U, Corno A, Nava S, Guccione P, Calabrò R, Marcelletti C (1990) Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome. Am J Dis Child 144:1120-1122
    • (1990) Am J Dis Child , vol.144 , pp. 1120-1122
    • Marino, B.1    Vairo, U.2    Corno, A.3    Nava, S.4    Guccione, P.5    Calabrò, R.6    Marcelletti, C.7
  • 27
    • 0018358812 scopus 로고
    • Conotruncal malformation complex: Examples of possible monogenic inheritance
    • Miller ME, Smith DW (1979) Conotruncal malformation complex: examples of possible monogenic inheritance. Pediarics 63:890-893
    • (1979) Pediarics , vol.63 , pp. 890-893
    • Miller, M.E.1    Smith, D.W.2
  • 29
    • 0032565859 scopus 로고    scopus 로고
    • Smad2 role in mesoderm formation, left-right patterning and craniofacial development
    • Nomura M, Li E (1998) Smad2 role in mesoderm formation, left-right patterning and craniofacial development. Nature 393:786-790
    • (1998) Nature , vol.393 , pp. 786-790
    • Nomura, M.1    Li, E.2
  • 30
    • 0014334454 scopus 로고
    • Multifactorial inheritance hypothesis for the etiology of congenital heart disease. The genetic environmental interaction
    • Nora JJ (1968) Multifactorial inheritance hypothesis for the etiology of congenital heart disease. The genetic environmental interaction. Circulation 38:604-617
    • (1968) Circulation , vol.38 , pp. 604-617
    • Nora, J.J.1
  • 32
    • 0023848717 scopus 로고
    • Update on counselling the family with a first-degree relative with a congenital heart defect
    • Nora JJ, Nora AH (1988) Update on counselling the family with a first-degree relative with a congenital heart defect. Am J Med Genet 29:137-142
    • (1988) Am J Med Genet , vol.29 , pp. 137-142
    • Nora, J.J.1    Nora, A.H.2
  • 34
    • 0002423312 scopus 로고
    • Late fetal development of retinoic acid-induced transposition of the great arteries: Morphology, physiology and biochemistry
    • Clark EB, Markwald RR, Takao A, eds, Futura Publishing Company, New York pp
    • Pexieder T, Blanc O, Pelouch V, Ostadalova I, Milerova M, Ostadal B (1995) Late fetal development of retinoic acid-induced transposition of the great arteries: Morphology, physiology and biochemistry. In: Clark EB, Markwald RR, Takao A, (eds) Developmental mechanism of heart disease. Futura Publishing Company, New York pp 297-307
    • (1995) Developmental mechanism of heart disease , pp. 297-307
    • Pexieder, T.1    Blanc, O.2    Pelouch, V.3    Ostadalova, I.4    Milerova, M.5    Ostadal, B.6
  • 38
    • 0018098793 scopus 로고
    • The recurrence risk in congenital heart disease
    • Sanchez-Cascos A (1978) The recurrence risk in congenital heart disease. Eur J Cardiol 7:197-210
    • (1978) Eur J Cardiol , vol.7 , pp. 197-210
    • Sanchez-Cascos, A.1
  • 41
    • 33748597974 scopus 로고    scopus 로고
    • Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect
    • Sarkozy A, Lepri F, Marino B, Pizzuti A, Digilio MC, Dallapiccola B (2006) Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect. Am J Med Genet 140(A):1970-1972
    • (2006) Am J Med Genet , vol.140 , Issue.A , pp. 1970-1972
    • Sarkozy, A.1    Lepri, F.2    Marino, B.3    Pizzuti, A.4    Digilio, M.C.5    Dallapiccola, B.6
  • 47
    • 0020440524 scopus 로고
    • Pregnancy and its outcome in women with and without surgical treatment of congenital heart disease
    • Whittemore R, Hobbins JC, Engle MA (1982) Pregnancy and its outcome in women with and without surgical treatment of congenital heart disease. Am J Cardiol 50:641-651
    • (1982) Am J Cardiol , vol.50 , pp. 641-651
    • Whittemore, R.1    Hobbins, J.C.2    Engle, M.A.3
  • 49
    • 0025863349 scopus 로고
    • The inheritance of conotruncal malformations: A review and report of two siblings with tetralogy of Fallot and pulmonary atresia
    • Wulfsberg EA, Zintz EJ, Moore JW (1991) The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot and pulmonary atresia. Clin Genet 40:12-16
    • (1991) Clin Genet , vol.40 , pp. 12-16
    • Wulfsberg, E.A.1    Zintz, E.J.2    Moore, J.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.