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Vol. 31. Núm. 9.
Páginas 314-322 (Enero 2004)
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Vol. 31. Núm. 9.
Páginas 314-322 (Enero 2004)
Acceso a texto completo
El diagnóstico genético preimplantacional y sus nuevas indicaciones en reproducción asistida
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C. Rubio1, L. Rodrigo1, A. Mercader1, E. Mateu1, C. Simón1,2, J Remohí1,2, A Pellicer1,2,3
1 Instituto Valenciano de Infertilidad (IVI). Valencia. España.
2 Departamento de Pediatría, Obstetricia y Ginecología. Universidad de Valencia. Valencia. España.
3 Hospital Universitario Dr. Peset. Valencia. España.
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Bibliografía
[1.]
RG Edwards, RL. Gardner.
Sexing of five rabbit blastocysts.
Nature, 214 (1968), pp. 576-577
[2.]
AH Handyside, EH Kontogianni, K Hardy, RML. Winston.
Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification.
Nature, 344 (1990), pp. 768-770
[3.]
K. Sermon.
Current concepts in preimplantation genetic diagnosis (PGD): a molecular biologist’s view.
Hum Reprod Update, 8 (2002), pp. 11-20
[4.]
DK Griffin, AH Handyside, RJA Penketh, RML Winston, JDA. Delhanty.
Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes.
Hum Reprod, 6 (1991), pp. 101-105
[5.]
A Veiga, J Santaló, F Vidal, C Calderón, C Giménez, M Boada, et al.
Twin pregnancy after preimplantation diagnosis for sex selection.
Hum Reprod, 9 (1994), pp. 2156-2159
[6.]
PN Scriven, AH Handyside, CM. Ogilvie.
Chromosome translocations modes and strategies for preimplantation genetic diagnosis.
Prenat Diagn, 18 (1998), pp. 1437-1449
[7.]
S Munné, C Magli, M Bahce, J Fung, M Legator, L Morrison, et al.
Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13,14,15,16,18,21,22.
Prenat Diagn, 18 (1998), pp. 1459-1466
[8.]
ESHRE Preimplantation Genetic Diagnosis Consortium: data collection III (May 2001.
Hum Reprod, 17 (2002), pp. 233-246
[9.]
K Hardy, KL Martin, HJ Leese, et al.
Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage.
Hum Reprod, 5 (1990), pp. 708-714
[10.]
MC Magli, L Gianaroli, AP Ferraretti, et al.
Rescue of implantation potential in embryos with poor prognosis by assisted zona hatching.
Hum Reprod, 13 (1998), pp. 1331-1335
[11.]
C Simón, A Mercader, J Garcia-Velasco, et al.
Cocultured of human embryos with autologous human endometrial epithelial cells in patients with implantation failure.
J Clin Endocrinol Metab, 84 (1999), pp. 2638-2646
[12.]
B Shapiro, KS Richter, DC Harris, ST. Daneshmand.
Dramatic declines in implantation and pregnancy rates in patients who undergo repeated cycles of in vitro fertilization with blastocyst transfer after one or more failed attempts.
Fertil Steril, 76 (2001), pp. 538-542
[13.]
L Gianaroli, MC Magli, AP Ferraretti, et al.
Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos.
Fertil Steril, 68 (1998), pp. 1128-1131
[14.]
T Pehlivan, C Rubio, L Rodrigo, J Romero, J Remohí, C Simón, A. Pellicer.
Impact of preimplantation genetic diagnosis on IVF outcome in implantation failure patients.
RBMOnline, 6 (2003), pp. 232-237
[15.]
M Sandalinas, S Sadowy, M Alikani, G Calderón, J Cohen, S. Munné.
Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage.
Hum Reprod, 16 (2001), pp. 1954-1958
[16.]
C Rubio, C Simón, F Vidal, L Rodrigo, T Pehlivan, J Remohí, et al.
Chromosomal abnormalities and embryo development in recurrent miscarriage couples.
Hum Reprod, 18 (2003), pp. 182-188
[17.]
GM. Stirrat.
Recurrent miscarriage I: definition and epidemiology, causes and management.
Lancet, 336 (1990), pp. 673-675
[18.]
P Tho, JR Byrd, PG. McDonough.
Etiologies and subsequent reproductive performance of 100 couples with recurrent abortion.
Fertil Steril, 32 (1979), pp. 389-395
[19.]
C. Coulam.
Unexplained recurrent pregnancy loss.
Clin Obstet Gynecol, 29 (1996), pp. 999-1004
[20.]
K Clifford, R Rai, H Watson, L. Regan.
An informative protocol for the investigation of recurrent miscarriage: preliminary experience of 500 consecutive cases.
Hum Reprod, 9 (1994), pp. 1328-1332
[21.]
L Plouffe, EW White, SP Tho, et al.
Etiological factors of recurrent abortion and subsequent reproductive performance of couples: have we made any progress in the past 10 years?.
Am J Obstet Gynecol, 167 (1992), pp. 313-321
[22.]
B Eiben, I Bartels, S Bahr-Porch, S Borgmanns, G Gatz, G Gellert, et al.
Cytogenetic analysis of 750 spontaneous abortions with the direct preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage.
Am J Hum Genet, 47 (1990), pp. 656-663
[23.]
CM Strom, N Ginsberg, M Applebaum, N Bozorgi, M White, M Caffarelli, et al.
Analysis of first trimester spontaneous abortions by chorionic villus sampling and karyotype.
J Assist Reprod Genet, 9 (1992), pp. 458-461
[24.]
TJ Hassold, N Chen, T Funkhouser, et al.
A cytogenetic study of 1000 spontaneous abortions.
Ann Hum Genet, (1998;v44), pp. 151-178
[25.]
MD Stephenson, KA Awartani, WP. Robinson.
Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case-control study.
Hum Reprod, 17 (2002), pp. 446-451
[26.]
M Ryynänem, S Leskinen, S Heinonen, P. Kirkinen.
Recurrence risk of a serious, noninherited chromosomal abnormality.
Fertil Steril, 68 (1997), pp. 439-442
[27.]
FS Cowchock, Z Gibas, LG. Jackson.
Chromosome errors as a cause of spontaneous abortion: the relative importance of maternal age and obstetric history.
Fertil Steril, 59 (1993), pp. 1011-1015
[28.]
JJ Stern, AD Dorfmann, AJ Gutiérrez-Nájar, M Cerrillo, CB. Coulam.
Frequency of abnormal karyotypes among abortuses from women with and without a history of recurrent spontaneous abortion.
Fertil Steril, 65 (1996), pp. 250-253
[29.]
W Warburton, J Kline, Z Stein, M Hutzler, A Chin, T. Hassold.
Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions.
Am J Hum Genet, 41 (1987), pp. 465-483
[30.]
M Ogasawara, K Aoki, S Okada, K. Suzumori.
Embryonic karyotype of abortuses in relation to the number of previous miscarriages.
Fertil Steril, 73 (2000), pp. 300-304
[31.]
F Vidal, C Giménez, C Rubio, C Simón, A Pellicer, J Santaló, et al.
FISH preimplantation diagnosis of chromosome aneuploidy in recurrent pregnancy wastage.
J Assist Reprod Genet, 15 (1998), pp. 309-312
[32.]
C Simón, C Rubio, F Vidal, C Giménez, C Moreno, JJ Parrilla, et al.
Increased chromosome abnormalities in preimplantation embryos after in-vitro fertilization in patients with recurrent miscarriage.
Reprod Fertil Dev, 1 (1998), pp. 87-92
[33.]
A Pellicer, C Rubio, F Vidal, Y Mínguez, C Giménez, J Egozcue, et al.
In vitro fertilization plus preimplantation genetic diagnosis in patients with recurrent miscarriage: an analysis of chromosome abnormalities in human preimplantation embryos.
Fertil Steril, 71 (1999), pp. 1033-1039
[34.]
AJ Wilcox, CR Weinberg, JF O’Connor, DD Baird, JP Schlatterer, RE Canfield, et al.
Incidence of early loss of pregnancy.
N Engl J Med, 319 (1998), pp. 189-194
[35.]
MJ Zinaman, ED Clegg, CC Browm, J O’Connor, SG. Selevan.
Estimates of human fertility and pregnancy loss.
Fertil Steril, 65 (1996), pp. 503-509
[36.]
L Werlin, I Rodi, A De Cherney, E Marello, D Hill, S. Munné.
Preimplantation genetic diagnosis as both a therapeutic and diagnostic tool in assisted reproductive technology.
Fertil Steril, 80 (2003), pp. 467-468
[37.]
SH Chen, S. Munné.
Can preimplantation genetic diagnosis (PGD) reduce the risk for recurrent pregnancy loss?.
Postgrad Obstet Gynecolo, 23 (2003), pp. 1-5
[38.]
MC Lanasa, WA Hogge, CJ Kubik, RB Ness, J Harger, T Nagel, et al.
A novel X chromosome-linked genetic cause of recurrent spontaneous abortion.
Am J Obstet Gynecol, 9 (2001), pp. 563-568
[39.]
S Uehara, M Hashiyada, K Sato, K Fujimori, K. Okamura.
Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss.
kFertil Steril, 76 (2001), pp. 908-914
[40.]
L Voullaire, H Slater, R Williamson, L. Wilton.
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization.
Hum Genet, 106 (2000), pp. 210-217
[41.]
D Wells, T Escudero, B Levy, K Hirschhorn, JDA Delhanty, S. Munné.
First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.
Fertil Steril, 78 (2002), pp. 543-549
[42.]
L Wilton, L Voullaire, P Sargeant, R Williamson, J. McBain.
Preimplantation aneuploidy screening using comparative genomic hybridization or fluorescence in situ hybridization of embryos from patients with recurrent implantation failure.
Fertil Steril, 80 (2003), pp. 860-868
[43.]
J Balasch, M Creus, F Fábregues, S Cívico, F Carmona, J Martorell, et al.
In-vitro fertilization treatment for unexplained recurrent abortion: a pilot study.
Hum Reprod, 11 (1996), pp. 1579-1582
[44.]
A Raziel, A Herman, D Strassburger, Y Soffer, I Bukowsky, R. Ron-El.
The outcome of in vitro fertilization in unexplained habitual aborters concurrent with secondary infertility.
Fertil Steril, 67 (1997), pp. 88-92
[45.]
J Remohí, E Gallardo, M Levy, D Valbuena, Santos MJ De los, C Simón, et al.
Oocyte donation in women with recurrent pregnancy loss.
Hum Reprod, 11 (1997), pp. 2048-2051
[46.]
NS Macklon, JPM Geraedts, BCJM. Fauser.
Conception to ongoing pregnancy: the «black box» of early pregnancy loss.
Hum Reprod Update, 8 (2002), pp. 333-343
[47.]
S Quenby, G Vince, R Farquharson, J. Aplin.
Recurent miscarriage: a defect in nature’s quality control?.
Hum Reprod, 17 (2002), pp. 1959-1963
[48.]
A Raziel, S Friedler, M Schahter, D Strassburger, R. Ron-El.
Succesful pregnancy after 24 consecutive fetal losses: lessons learned from surrogacy.
Fertil Steril, 74 (2000), pp. 104-106
[49.]
P Nicolaidis, MB. Petersen.
Origin and mechanisms of nondisjunction in human autosomal trisomies.
Hum Reprod, 13 (1998), pp. 313-319
[50.]
PA Jacobs, TJ. Hassold.
The origin of numerical chromosome abnormalities.
Adv Genet, 33 (1995), pp. 101-133
[51.]
AC. Chandley.
The origin of chromosomal aberrations in man and their potential for survival and reproduction in the adult human populations.
Ann Genet, 24 (1981), pp. 5-11
[52.]
LC Reinisch, KL Silver, KW. Dumars.
Sex chromosome mosaicism in couples with repeated fetal loss [abstract].
Am J Hum Genet, 33 (1981), pp. 117
[53.]
MV Zaragoza, U Surti, RW Redline, E Millie, A Chakravarti, TJ. Hassold.
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry.
Am J Hum Genet, 66 (2000), pp. 1807-1820
[54.]
S Egozcue, J Blanco, F Vidal, J. Egozcue.
Diploid sperm and the origin of triploidy.
Hum Reprod, 17 (2002), pp. 5-7
[55.]
D McFadden, R Jiang, S Langlois, WP. Robinson.
Dispermy: origin of diandric triploidy.
Hum Reprod, 17 (2002), pp. 3037-3038
[56.]
U Eichenlaub-Ritter, S Cucurkam, I. Betzendahl.
Studies on the aneugenic properties of trichlorfon, a pesticide, vermicide and drug used in the treatment of Alzheimer patients [abstract book 1].
Hum Reprod, 14 (1999), pp. 240-241
[57.]
CG Roberts, O’Neill.
Increase in the rate of diploidy with maternal age in unfertilised in-vitro fertilization oocytes.
Hum Reprod, 10 (1995), pp. 2139-2141
[58.]
M De Braekeleer, TN. Dao.
Cytogenetic studies in couples experiencing repeated pregnancy losses.
Hum Reprod, 5 (1990), pp. 519-528
[59.]
T Hassold, PA Hunt, S. Sherman.
Trisomy in humans: incidence, origin and etiology.
Curr Opin Genet Develop, 3 (1993), pp. 398-403
[60.]
J Pfeffer, MG Pang, SF Hoegerman, CJ Osgood, MW Stacey, J Mayer, et al.
Aneuploidy frequencies in semen fractions from ten oligoasthenoteratozoospermic patients donating sperm for intracytoplasmic sperm injection.
Fertil Steril, 72 (1999), pp. 472-478
[61.]
B Arán, J Blanco, F Vidal, JM Vendrell, S Egozcue, PN Barri, et al.
Screening for abnormalities of chromosomes X,Y and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program.
Fertil Steril, 72 (1999), pp. 696-701
[62.]
MG Pang, SF Hoegerman, AJ Cuticchia, SY Moon, GF Doncel, AA Acosta, et al.
Detection of aneuploidy for chromosomes 4,6,7,8,9,10,11,12,13,17,18,21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenozoospermia undergoing intracytoplasmic sperm injection.
Hum Reprod, 14 (1999), pp. 1266-1273
[63.]
M Plachot, A Veiga, J Montagut, J De Grouchy, G Calderón, S Lepretre, et al.
Are clinical and biological IVF parameters correlated with chromosomal disorders in early life: a multicentric study.
Hum Reprod, 3 (1988), pp. 627-635
[64.]
L Gianaroli, MC Magli, AP Ferraretti, S. Munné.
Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed.
Fertil Steril, 72 (1999), pp. 837-844
[65.]
M Sandalinas, C Márquez, S. Munné.
Spectral karyotyping of fresh, non-inseminated oocytes.
Mol Hum Reprod, 8 (2002), pp. 580-585
[66.]
K Bajnóczky, S. Gardó.
premature anaphase» in a couple with recurrent miscarriages.
Hum Genet, 92 (1993), pp. 388-390
[67.]
D Manor, S Kol, N Lewit, A Lightman, D Stein, M Pillar, et al.
Undocumented embryos: do not trash them, FISH them.
Hum Reprod, 11 (1996), pp. 2502-2506
[68.]
D Manor, D Stein, J. Itskovitz-Eldor.
Preimplantation diagnosis by FISH: the Rambam experience.
J Assist Reprod Genet, 15 (1998), pp. 308-309
[69.]
M Vandervorst, I Liebaers, K Sermon, C Staessen, A De Vos, Velde H Van de, et al.
Successful preimplantation genetic diagnosis is related to the number of available cumulusoocyte complexes.
Hum Reprod, 13 (1998), pp. 3169-3176
[70.]
S Munné, HUG Weier, J Grifo, J. Cohen.
Chromosome mosaicism in human embryos.
Biol Reprod, 51 (1994), pp. 373-379
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