A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome

47 XXY/46 XX mosaicism with characteristics suggesting Klinefelter syndrome is very rare and at present, only seven cases have been reported in the literature.

Source: International Journal of Pediatric Endocrinology - June 2, 2016 Category: Endocrinology Authors: Noor Shafina Mohd Nor and Muhammad Yazid Jalaludin Source Type: research