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Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease
Author(s) -
Renbaum P.,
Brooks B.,
Kaplan Y.,
EldarGeva T.,
Margalioth E J.,
LevyLahad E.,
Altarescu G.
Publication year - 2007
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1668
Subject(s) - alagille syndrome , genetics , disease , polar body , biology , medicine , pathology , gene , cholestasis , meiosis
Objective The development of a preimplantation genetic diagnosis (PGD) protocol for Alagille syndrome (AGS), a rare autosomal dominant disorder with hepatic, cardiac and ophthalmologic involvement. Methods We developed a polar body (PB)‐based multiplex fluorescent PCR reaction for a female affected with AGS. The protocol included analysis of the Jagged 1 ( JAG1 ) familial mutation and five closely linked highly polymorphic markers (D20S162, D20S901, D20S894, and D20S186). Results In two cycles of PGD 9 of ten embryos were accurately diagnosed by assessment of first and second PBs, one embryo required additional blastomere biopsy. Conclusions This protocol takes advantage of the larger window of opportunity for transfer and the increased accuracy of diagnosis afforded by the combination of PB biopsy and multiple marker analysis. Two cycles resulted in the transfer of two and three mutation‐free embryos and a subsequent pregnancy as measured by the rising hCG levels. Copyright © 2007 John Wiley & Sons, Ltd.