A novel C-terminal truncating NR5A1 mutation in dizygotic twins

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Abstract

Nuclear receptor subfamily 5, group A, member 1 (NR5A1) is a nuclear receptor involved in gonadal and adrenal development. We identified a novel C-terminally truncating NR5A1 mutation, p.Leu423Trpfs∗7, in dizygotic twins with 46,XY disorders of sex development. Our results highlight the functional importance of C-terminal region of NR5A1 and indicate that NR5A1 mutations can be associated with intrafamilial phenotypic variations, progressive testicular dysfunction, hypogonadotropic hypogonadism, and borderline adrenal dysfunction.

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Hattori, A., Zukeran, H., Igarashi, M., Toguchi, S., Toubaru, Y., Inoue, T., … Fukami, M. (2017). A novel C-terminal truncating NR5A1 mutation in dizygotic twins. Human Genome Variation, 4. https://doi.org/10.1038/hgv.2017.8

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