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    Detection of Mutations in the CYP21A2 Gene: Genotype-Phenotype Correlation in Slovenian Couples with Conceiving Problems

    December 2015 in “ Balkan Journal of Medical Genetics
    Špela Stangler Herodež, L Fijavž, Boris Zagradišnik, Nadja Kokalj Vokač
    Studysummary This study found no significant difference in the prevalence of CYP21A2 mutations between couples with unexplained fertility problems and healthy controls, but identified an association between the c.290-13A/C>G mutation and clinical issues like hormone deviations and polycystic ovary syndrome.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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    Research cited in this study 2

    1. Reproductive Outcomes of Female Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Indian Journal of Endocrinology and Metabolism · 2013
    2. Recommendations for Treatment of Nonclassic Congenital Adrenal Hyperplasia: An Update Steroids · 2011