Información de la revista
Vol. 52. Núm. 5.
Páginas 485-487 (mayo 2000)
Vol. 52. Núm. 5.
Páginas 485-487 (mayo 2000)
Acceso a texto completo
La resonancia magnética en un recién nacido con agenesia de válvula pulmonar y deleción del cromosoma 22q 11,2
Visitas
6992
Este artículo ha recibido
Información del artículo
El Texto completo está disponible en PDF
Biblografía
[1.]
N. Chevers.
Recherches sur les maladies de l'artère pulmonaire.
Arch Gen Med, 15 (1847), pp. 488-508
[2.]
F. Godart, C. Rey, G.M. Breviere, C. Francort, G. Vaskmann.
Le agenesie des valves pulmonaires. Experience sur 20 annes.
Arch Mal Coeur, 88 (1995), pp. 673-679
[3.]
D.A. Driscoll, M.L. Budarf, B.S. Emanuel.
A genetic etiology for DiGeorge syndrome: Consistent deletion and microdeletion of 22q11.
Am J Hum Genet, 50 (1992), pp. 924-933
[4.]
P.Y. Scambler, D. Kelly, E. Lindsay, R. Willianson, R. Goldberg, R. Shprintzen, et al.
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.
Lancet, 339 (1992), pp. 1138-1139
[5.]
E. Goldmunta, D.A. Driscoll, M.L. Budarf, E.M. Zackai, D.M. McDonal-McGinn, J.A. Biegel, et al.
Microdeletion of chromosomal region 22q11 in infant with congenital cardiac defects.
J Med Genet, 30 (1993), pp. 807-812
[6.]
J.C. Fouron, D.Y. Sahn, R. Bender, R. Block, H. Schreider, P. Fromberger, et al.
Prenatal diagnosis and circulatory characteristics in tetralogy of Fallot with absent pulmonary valve.
Am J Cardiol, 64 (1989), pp. 547-549
[7.]
H. Frank, V. Salzer, C. Popow, R. Stiglbauer, G. Wolleneck, H. Innhof.
Magnetic resonance imaging of absent pulmonary valve syndrome.
Pediatr Cardiol, 17 (1996), pp. 35-39
[8.]
D.I. Wilson, Y.A. Goodship, Y.A. Goodship, Y. Burn, I.E. Croes, P.Y. Scambler.
Deletion within chromosome 22q11 in familial congenital heart disease.
Lancet, 340 (1992), pp. 573-575
[9.]
Mc. Johnson, A.W. Strauss, S.B. Dowton, T.L. Spray, C.B. Huddleston, M.K. Wood, et al.
Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome.
Am J Cardiol, 76 (1995), pp. 66-69
[10.]
H. Horigome, T. Takamo, T. Hiramo, T. Kajima, S. Ohtami.
Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve.
Am J Med Genet, 38 (1991), pp. 608-611
[11.]
E. Di Segui, S. Einzig, Y.L. Bass, Y.E. Edward.
Congenital absence of pulmonary valve associated with tetralogy of Fallot: Diagnosis by 2-dimensional echocardiography.
Am J Cardiol, 51 (1983), pp. 1789-1800
Copyright © 2000. Asociación Española de Pediatría