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47, XYY mosaic karyotype and congenital absence of bilateral vas deferens
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posted on 2022-01-24, 07:22
authored by
Ci Zou
Ci Zou
,
Dexin Yin
,
Hao Geng
,
Xiaofeng Lan
,
Wei Sun
Wei Sun
We report a rare case of infertility presenting with a 47, XYY mosaicism and congenital bilateral absence of vas deferens. With our patient's informed written consent, we performed a complete set of genetic tests for male infertility.
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Genetics not elsewhere classified
Developmental genetics (incl. sex determination)
Keywords
47, XYY syndrome
Ongenital absence
bilateral vas deferens
Genetics
Developmental Genetics (incl. Sex Determination)
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GPL
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