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. 2021 Sep;41(10):1255-1257.
doi: 10.1002/pd.5890. Epub 2021 Jan 19.

Increased RISK for 47,XXY on cell-free DNA screen: Not always Klinefelter syndrome

Luisa Ronzoni  1 , Maria Francesca Bedeschi  1 , Gaia Silibello  2 , Veronica Accurti  3 , Marina Di Segni  4 , Valeria Nicotra  1 , Paola Vizziello  2 , Faustina Lalatta  1
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Increased RISK for 47,XXY on cell-free DNA screen: Not always Klinefelter syndrome

Luisa Ronzoni et al. Prenat Diagn. 2021 Sep.
No abstract available

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References

REFERENCES

    1. Kanakis GA, Nieschlag E. Klinefelter sundrome: more than hypogonadism. Metabolism Clin Exp. 2018;86:135-144.
    1. Nieschlag E. Klinefelter syndrome: the commonest form of hypogonadism, but often overlooked or untreated. Dtsch Arztebl Int. 2013;110:347-353.
    1. Zampini L, Burla T, Silibello G, et al. Early communicative skills of children with Klinefelter syndrome. Clin Linguist Phon. 2018;32(7):577-586.
    1. Lalatta F, Tint GS. Counseling parents before prenatal diagnosis: do we need to say more about the sex chromosome aneuploidies? Am J Med Genet. 2013;161A:2873-2879.
    1. Samango-Sprouse C, Keen C, Sadeghin T, et al. The benefits and limitations of cell-free DNA screening for 47, XXY (klinefelter syndrome). Prenat Diagn. 2017;37(5):497-501.

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