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Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype  Gulseren Bagci, Ph.D., Atil.

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Presentation on theme: "Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype  Gulseren Bagci, Ph.D., Atil."— Presentation transcript:

1 Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype  Gulseren Bagci, Ph.D., Atil Bisgin, M.D., Ph.D., Sibel Berker Karauzum, Ph.D., Bilal Trak, M.D., Guven Luleci, Ph.D.  Fertility and Sterility  Volume 95, Issue 5, Pages 1786.e e3 (April 2011) DOI: /j.fertnstert Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions

2 Figure 1 Family pedigree. There are three cases in the family: two sisters and their mother's maternal aunt. Fertility and Sterility  , 1786.e e3DOI: ( /j.fertnstert ) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions

3 Figure 2 Multiplex polymerase chain reaction results on ethidium bromide–stained 4% agarose gel for the patients, with no amplification in SY14, gene SRY. In each group, from left to right, lane 1 is the negative control, lane 2 is the father of the proband (III-1), lane 3 is the proband (IV-1), lane 4 is the mother of the proband (III-2), lane 5 is the positive control, and lane 6 is the marker. Fertility and Sterility  , 1786.e e3DOI: ( /j.fertnstert ) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions


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