Successful pregnancy after preimplantation genetic diagnosis in a female with Robertsonian translocation

Journal of the Formosan Medical Association

Volumn 103, Issue 8, 2004, Pages 637-639

  Wu, Yueh Chao ^a   Chen, Chun Kai ^a   Huang, Hong Yuan ^a   Chou, Chi Ju ^a   Soong, Yung Kuei ^a  

^a CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

Author keywords

Case reports; Fluorescence in situ hybridization; Preimplantation diagnosis; Translocation (genetics)

Indexed keywords

CHORIONIC GONADOTROPIN; LEUPRORELIN; RECOMBINANT FOLLITROPIN;

ADULT; AMNIOCENTESIS; ARTICLE; ASPIRATION; BIOPSY; BLASTOMERE; CASE REPORT; CESAREAN SECTION; EMBRYO; EMBRYO TRANSFER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GESTATIONAL AGE; HUMAN; OOCYTE; OVARY CYCLE; PHYSICAL EXAMINATION; PREGNANCY; PRENATAL DIAGNOSIS; PUERPERIUM; RECURRENT ABORTION; ROBERTSONIAN CHROMOSOME TRANSLOCATION; TISSUE FIXATION; TWIN PREGNANCY;

ABORTION, HABITUAL; ABORTION, SPONTANEOUS; ADULT; BLASTOCYST; FEMALE; FERTILIZATION IN VITRO; HUMANS; KARYOTYPING; PREGNANCY; PREGNANCY OUTCOME; PREIMPLANTATION DIAGNOSIS; TRANSLOCATION, GENETIC;

EID: 8344285148     PISSN: 09296646     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)

1. Gardner RJM, Sutherland GR: Chromosome abnormalities and genetic counseling. 3rd ed. Oxford: Oxford University Press; 2004: 122-37.
2. Scriven PN, Flinter FA, Braude PRB, et al: Robertsonian translocation-reproductive risks and indications for preimplantation genetic diagnosis. Hum Reprod 2001;16:2267-73.
3. Handyside A, Kontogianni E, Hardy K, et al: Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature 1990;344:768-70.
4. Conn CM, Harper JC, Winston RML, et al: Infertile couples with Robertsonian translocation: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions. Hum Genet 1998; 102:117-23.
5. Chen CK, Shen GY, Horng SG, et al: The relationship of pronuclear stage morphology and chromosome status at cleavage stage. J Assist Reprod Genet. In press 2004.
6. Harper JC, Delhanty JD: FISH in preimplantation diagnosis. In: J Walker, ed. Methods in molecular biology, molecular diagnosis of genetic disease. New Jersey: Human Press, 1996:259-68.
7. Harper JC, Delhanty JD: Detection of chromosomal abnormalities in human preimplantation embryos using FISH. J Assist Reprod Genet 1996;13:137-9.
8. Harper JC, Coonen E, Handyside AH, et al: Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic, preimplantation human embryos. Prenat Diagn 1995;15:41-9.
9. Hopman AH, Ramaekers FC, Raap AK, et al: In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors. Histochemistry 1988;89:307-16.
10. Dutrillaux B, Lejeune J: Study of progeny of individuals bearing a t(DqDq) translocation. Ann Genet 1970;13:11-8.
11. Stern C, Pertile M, Norris H, et al: Chromosome translocations in couples with in-vitro fertilization implantation failure. Hum Reprod 1999;14:2097-101.
12. Tsui KM, Yu WL, Lo FM, et al: A cytogenetic study of Chinese couples with recurrent spontaneous abortion. Chin Med J (Engl) 1996;109:635-8.
13. Fryns JP, Van Buggenhout G: Structural chromosome rearrangements in couples with recurrent fetal wastage. Eur J Obstet Gynecol Reprod Biol 1998;81:171-6.
14. ESHRE PGD Consortium Sterring Committee: ESHRE Preimplantation Genetic Diagnosis Consortium: data collection II (May 2000). Hum Reprod 2000;15:2673-83.
15. ESHRE PGD Consortium Sterring Committee: ESHRE Preimplantation Genetic Diagnosis Consortium: data collection III (May 2001). Hum Reprod 2002;17:236-46.
16. Van De Velde H, De Vos A, Sermon K, et al: Embryo implantation after biopsy of one or two cells from cleavage stage embryos with a view to PGD. Prenat Diagn 2000;20:1030-7.
17. American Society of Reproductive Medicine and Society for Assisted Reproductive Technology. Practice Committee Report. Preimplantation genetic diagnosis. Released June 2001.