Albu Cristina Crenguţa, Albu Dinu Florin, Muşat Ana Roxana, Stancu Ioana Georgeta, Albu Ştefan Dimitrie, Pătraşcu Anca, Gogănău Alexandru Marian
Department of Genetics, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania;
Rom J Morphol Embryol. 2019;60(4):1311-1316.
Prenatal diagnosis of disorder of sex development (DSD) is very rare and is estimated to occur in 1∕2500 pregnancies. A group of DSDs are the 46,XX testicular DSD. Today, the incidence of 46,XX testicular DSD is estimated at 1∕20 000 newborn males. A majority of males with DSD have an unbalanced X;Y exchange involving the pseudoautosomal region, with translocation of the sex-determining region of the Y (SRY) gene onto Xp23.3. We present a rare case of very early prenatal diagnosis and management of a fetus with SRY-positive 46,XX testicular DSD.
性发育障碍(DSD)的产前诊断非常罕见,据估计在每2500次妊娠中发生1例。46,XX睾丸型DSD是DSD的一种类型。如今,46,XX睾丸型DSD的发病率估计为每20000例新生男婴中有1例。大多数患有DSD的男性存在涉及假常染色体区域的X;Y不平衡交换,导致Y染色体的性别决定区域(SRY)基因易位到Xp23.3。我们报告了1例罕见的胎儿SRY阳性46,XX睾丸型DSD的极早期产前诊断及处理病例。