A novel variant in LCHGR gene in 3 siblings with type 1 Leydig cell hypoplasia
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DOI: 10.1080/09513590.2020.1789859
Abstract: Abstract Introduction Leydig cell hypoplasia (LCH) is an autosomal recessive disease that causes 46, XY sex development disorder. The patients with LCH are usually in the female phenotype and are presented with the complaints of… read more here.
Keywords: leydig cell; primary amenorrhea; novel variant; female phenotype ... See more keywords