Literature DB >> 12831599

Preimplantation genetic diagnosis for familial dysautonomia.

S Rechitsky1, O Verlinsky, A Kuliev, R S Ozen, C Masciangelo, A Lifchez, Y Verlinsky.   

Abstract

Familial dysautonomia (FD) is the most common congenital sensory neuropathy in Ashkenazi Jews, caused by a single major mutation in the IKBKAP gene. Effective management for this severe debilitating disease is still not available, making preimplantation genetic diagnosis (PGD) a useful option for at-risk couples to establish an FD free pregnancy from the outset. PGD was performed for a couple with a previous affected child with FD, using first and second polar body testing to preselect mutation-free oocytes, based on mutation analysis with simultaneous testing of two closely linked markers, D9S58 and D9S1677. Of 15 tested oocytes, 11 carried information about both polar bodies' genotype, of which seven were predicted to be free of the FD gene. Three embryos resulting from these oocytes were transferred back to the patient, resulting in a triplet pregnancy and the birth of three unaffected children confirmed to be free of FD. This is the first PGD for FD, providing an alternative for those at-risk couples who cannot accept prenatal diagnosis and termination of pregnancy as an option for avoiding FD.

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Year:  2003        PMID: 12831599     DOI: 10.1016/s1472-6483(10)62172-4

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  1 in total

Review 1.  Preimplantation genetic diagnosis (PGD) for genetic prion disorder due to F198S mutation in the PRNP gene.

Authors:  Alice Uflacker; P Murali Doraiswamy; Svetlana Rechitsky; Tricia See; Michael Geschwind; Ilan Tur-Kaspa
Journal:  JAMA Neurol       Date:  2014-04       Impact factor: 18.302

  1 in total

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