Preimplantation Genetic Diagnosis (PGD) of Hereditary Cancer Syndromes
Authors:
L. Raszyková; V. Hořínová; P. Texl
Authors place of work:
Laboratoř lékařské genetiky, Sanatorium Helios, Brno
Published in the journal:
Klin Onkol 2012; 25(Supplementum): 84-86
Summary
Advances in molecular biology techniques made possible genotype analysis from one or several cells. This can be used in preimplantation genetic diagnosis (PGD) not only of chromosomal aneuploidy but also of single gene diseases as well as hereditary cancer syndromes. PGD can be a benefit for those cases when the risk of transfer of pathological alteration from parent to offspring is unwelcome. We submit three cases of PGD with the results.
Key words:
preimplantation genetic diagnosis – single gene disease – hereditary cancer syndromes – in vitro fertilization
The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study.
The Editorial board declares that the manuscript met the ICMJE “uniform requirements” for biomedical papers.
Submitted:
27. 4. 2012
Accepted:
25. 6. 2012
Zdroje
1. Wells D, Delhanty JD. Preimplantation genetic diagnosis: applications for molecular medicine. Trends Mol Med 2001; 7(1): 23–30.
2. Harton GL, De Rycke M, Fiorentino F et al. ESHRE PGD consortium best practise guidelines for amplification-based PGD. Hum Reprod 2011; 26(1): 33–40.
3. Hüttelová R, Kleibl Z, Řezáčová J et al. Předpoklady pro preimplantační genetickou diagnostiku (PGD) u nosičů mutací v nádorových predispozičních genech. Klin Onkol 2009; 22 (Suppl): 69–74.
4. De Boer K, MacArthur S, Murray C et al. First live birth following blastocyst biopsy and PGD analysis. Reprod Biomed Online 2002; 4: 35.
Štítky
Paediatric clinical oncology Surgery Clinical oncologyČlánok vyšiel v časopise
Clinical Oncology
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