Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/39151
Title: A teenager with a t(X;17)(q22;q25) and ovarian failure
Author: Martinez-Valenzuela, M.
Rivera, H.
Mundo-Ayala, J.N.
Gonzalez-Mercado, M.G.
Davalos-Rodriguez, I.P.
Issue Date: 2010
Abstract: Background: The effects of a balanced X;Autosome translocation [t(X;A)] on the fertility of carrier females led to the definition of the Xq13?q27 region as critical for ovarian function and reproductive lifespan. We describe here a teenager with ovarian failure likely due to a balanced t(X;17)(q22;q25). Case: The 16 year-old patient presented with secondary amenorrhea. She exhibited height of 164 cm, slender habitus, and sexual development Tanner 2. Methods: Hormonal determinations, GTG- and RBG-banded karyotypes, fluorescence in situ hybridization, and human androgen receptor assay. Results: FSH of 141 mIU/ml and LH of 46 mIU/ml); karyotype 46,X,t(X;17)(q22;q25)[30].ish der(X)t(X;17)(17qsubt el+); skewed inactivation of the normal X which was the maternal one as shown by the HUMARA assay. The maternal chromosomes were 46,XX; the father was unavailable. Conclusions: The patient's (X;17) translocation likely accounts for her ovarian failure via an epigenetic down-regulation of ovary expressed 17q25 genes relocated next to the Xq21 POF Critical Region 1 and related to ovarian development and function. Her otherwise inconspicuous phenotype agrees with the preferential inactivation of the normal X-chromosome that preserves the gene homeostasis in women with a balanced t(X;A). Finally, the normal maternal karyotype along with the HUMARA results and the sterility of males carrying a t(X;A) strongly suggests that this t(X;17) was a paternal de novo mutation.
URI: http://www.scopus.com/inward/record.url?eid=2-s2.0-77957732285&partnerID=40&md5=3df9f0f07addefac42c7b1059e8efe3c
http://hdl.handle.net/20.500.12104/39151
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