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Malformations Extracardiaques Associées à des Cardiopathies Congénitales (Etude statistique portant sur 1000 cas)

Published online by Cambridge University Press:  01 August 2014

I. Emerit ,
P. Vernant ,
P. Corone  and
J. de Grouchy
I. Emerit
Affiliation:
Clinique Cardiologique, Hôpital Broussais. Paris, (Prof. P. Soulié) Clinique de Génétique Médicale, Hôpital des Enfants Malades, Paris, (Prof. M. Lamy)
P. Vernant
Affiliation:
Clinique Cardiologique, Hôpital Broussais. Paris, (Prof. P. Soulié) Clinique de Génétique Médicale, Hôpital des Enfants Malades, Paris, (Prof. M. Lamy)
P. Corone
Affiliation:
Clinique Cardiologique, Hôpital Broussais. Paris, (Prof. P. Soulié) Clinique de Génétique Médicale, Hôpital des Enfants Malades, Paris, (Prof. M. Lamy)
J. de Grouchy
Affiliation:
Clinique Cardiologique, Hôpital Broussais. Paris, (Prof. P. Soulié) Clinique de Génétique Médicale, Hôpital des Enfants Malades, Paris, (Prof. M. Lamy)

Summary

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The authors have studied the frequency and nature of associated malformations in a series of 1000 patients with congenital heart disease. Etiological factors have been statistically analyzed, too.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 16 , Issue 1 , January 1967 , pp. 27 - 51
Copyright
Copyright © The International Society for Twin Studies 1967

References

Bibliographie

Abbott, M.E. (1927). Congenital heart disease. Nelson's Loose-Leaf Living Medicine, Vol. 4, New York.Google Scholar
Boesen, J. et al. (1963). Extracardiac congenital malformations in children with congenital heart disease. Acta Paed., Suppl., 146: 28.CrossRefGoogle Scholar
Campbell, M. (1961). Twins and congenital heart disease. A. Ge. Me. Ge., 10: 4.Google ScholarPubMed
Campbell, M. (1961). Place of maternal rubella in the aetiology of congenital heart disease. Brit. Med. J., 1: 691.Google Scholar
Campbell, M. (1963). The mode of inheritance in isolated laevocardia and dextrocardia and situs inversus. Brit. Heart J., 25: 803.Google Scholar
Carleton, R.A. (1958). Familial occurrence of congenital heart disease. New England J. Med., 259: 1237.Google Scholar
Cruveiller, J. et al. (1963). Contribution à l'étude des cardiopathies congénitales. Ann. Pediat., 10: 284.Google Scholar
Evans, T.N., Brown, G.C. (1963). Congenital anomalies and virus infections. Amer. J. Obstet. Gynec., 87: 749.Google Scholar
Emerit, I., Vernant, P. (1966). Syndrome de Goldenhar et malformation complexe du cœur. A propos d'une observation. Presse Med., 74: 507.Google Scholar
Emerit, I. et al. (1964). Communication interauriculaire, troubles du rythme et malformation des membres supérieurs. Un nouveau syndrome. Ann. Pediat., 63: 2560.Google Scholar
Emerit, I. et al. (1965). Malformations complexes des membres supérieurs associées à une cardiopathie congénitale. A. Ge. Me. Ge., 14: 132.Google Scholar
Farrar, J.F., Mackie, I.J. (1964). Survey of possible causes of congenital malformation. Med. J. Australia, 2: 702.Google Scholar
Fuhrmann, W. (1961). Untersuchungen zur Atiologie der angeborenen Angiokardiopathien. Acta Genet., 11: 289.Google Scholar
Gall, J.C. et al. (1966) Holt-Oram syndrome: clinical and genetic study of a large family. Amer. J. Hum. Genet., 18: 187.Google Scholar
Gibson, S., Clifton, W.M. (1938). Congenital heart disease. Amer. J. Dis. Child., 55: 761.Google Scholar
Grouchy, J. et al. (1963). Inversion péricentrique probable du chromosone N. 2 et malformations congénitales chez un garçon. Ann. Genet., 6: 21.Google Scholar
Grouchy, J. et al. (1965). Syndrome de Klinefelter chez un garçon trisomique 21. Presse Med., 73: 1209.Google Scholar
Grouchy, J. et al. (1966). Mosaïque XO/XY/Xy et syndrome de Turner chez une fille de 18 ans. Ann. Genet., 9: 86.Google Scholar
Hedberg, E. (1963). On relationship between maternal conditions during pregnancy and congenital malformations. Acta Paed. (Stockholm), 52: 353.Google Scholar
Higgins, I.T.T. (1965). The epidemiology of congenital heart disease. J. Chron. Dis., 18: 699.Google Scholar
Holmes, L.B. (1965). Congenital heart disease and upper extremity deformities. A report of two families. New England J. Med., 272: 437.Google Scholar
Holt, M., Oram, S. (1960) Familial heart disease with skeletal malformations. Brit. Heart J., 22: 236.Google Scholar
Ingalls, T.H., Klingberh, M.A. (1965). Congenital malformations. Clinical and community considerations. Amer. J. Med. Sci., 249: 316.Google ScholarPubMed
Kuhn, E. et al. (1963). Primary pulmonary hypertension, congenital heart disease and skeletal anomalies in three generations. Jap. Heart J., 4: 205.Google Scholar
Labbe, B. (1964). Apport de la génétique à l'étude étiologique des cardiopathies congénitales. Thèse. Paris.Google Scholar
Lamy, M. et al. (1957). Genetic and non-genetic factors in the etiology of congenital heart disease. A study of 1188 cases. Amer. J. Hum. Genet., 9: 17.Google Scholar
Lewis, K.B. (1964). Upper limb cardiovascular syndrome. Circulation, 30: 113.Google Scholar
McDomald, A.D. (cit. chez Ingalls).Google Scholar
McIntosh, R. et al. (1954). The incidence of congenital malformations: a study of 5964 pregnancies. Pediatrics, 14: 505.Google Scholar
McKeown, T. et al. (1953). The familial incidence of congenital malformations of the heart. Brit. Heart J., 15: 273.CrossRefGoogle Scholar
McKusick, V.A. (1960). Cardiovascular system. Med. Genet., 11.Google Scholar
McKusick, V.A. (1964). Genetics of cardiovascular disease. Circulation, 30: 326.CrossRefGoogle Scholar
McMahon, B. et al. (1953). The incidence and life expectation of children with congenital heart disease. Brit. Heart J., 15: 121.Google Scholar
Marden, P.M. et al. (1964). Congenital anomalies in the newborn infant, including minor variations. J. Pediat., 64: 357.Google Scholar
Neill, C. A., Strang, R.H. (1960). Familial study of congenital heart disease. Amer. J. Dis. Child., 100: 617.Google Scholar
Polani, P.E., Campbell, M. (1955). An aetiological study of congenital heart disease. Ann. Hum. Genet, 19: 209.Google Scholar
Pruzanski, W. (1964). Familial congenital malformations of the heart and upper limbs. A syndrome of Holt-Oram. Cardiologia, 45: 21.CrossRefGoogle ScholarPubMed
Richards, M.R. (1955). Congenital malformations of the cardiovascular system in a series of 6053 infants. Pediatrics, 15: 12.Google Scholar
Roskowski, J., Kietlinska, Z. (1965). Indirect causes of congenital malformations. An analysis of 212 cases. Gynaecologia, 159: 47.Google Scholar
Rowe, R.D. (1963). Maternal rubella and pulmonary artery stenosis. Report of 11 cases. Pediatrics, 32: 180.Google Scholar
Sayegh, C. (1963). Contribution à l'étude de l'étiologie des malformations congénitales. J. Genet. Hum., 12: 91 et 214.Google Scholar
Soulie, P. et al. (1965). Stenose aortique sus-valvulaire, faciès particulier et retard mental. A propos de trois observations. Bull. Mem. Soc. Hop., Paris, 116: 427.Google Scholar
Stanbury, J.B. et al. (1960). The Metabolic Basis of Inherited Disease. McGraw Hill, New York.Google Scholar
Stevenson, S.S. et al. (1950). 677 congenitally malformed infants and associated gestational characteristics. Pediatrics, 6: 27.Google Scholar
Vernant, P. et al. (1966). Le cœur dans le syndrome de Turner-Ullrich. Arch. Mal. Coeur, 53: 850.Google Scholar
Warkany, J., Kalter, H. (1961). Congenital malformations. New Engl. J. Med., 265: 993.Google Scholar
Weil, M.H., Allenstein, B.I. (1961). A report of congenital heart disease in five members of one family. New Engl. J. Med., 265: 661.Google Scholar
Wiland, O.K. (1956). Extracardiac anomalies in association with congenital heart disease. Lab. Invest., 5: 380.Google Scholar
Zetterqvist, P. (1963). The syndrome of familial atrial septal defect, heart arrythmia and hand malformation (Holt-Oram). Acta Paediat., 52: 1.Google Scholar