| Literature DB >> 29263053 |
Muhammad Riaz Khan1, Ihtisham Bukhari1,2, Tang Junxiang3, Liu Hui3, Niaz Muhammad4, Cui Fan5, Jiangsheng Zhu6, Mian Wu7.
Abstract
Sex chromosomal mosaicism has been considered as a major cause of human sexual differentiation disorders, like partial virilization and ambiguous genitalia. 45,X/46,XX, 45,X/46,XY and 46,XY/47,XXY are three most common sex chromosome mosaics associated with human ambiguous genitalia. Here, we report the case of a 3-year-old boy with ambiguous genitalia, bilateral cryptorchidism, and with an inguinal hernia. G banded cytological karyotyping and FISH analyses revealed that the patient has extremely rare and novel sex chromosome mosaic 45,X/45,Y/46,XY/46,YY/47,XYY karyotype. These cells exist in different percentages, important for phenotypic appearance of the patient. This is a first report of an unusual mosaic karyotype causing ambiguous genitalia.Entities:
Keywords: 45,X/45,Y/46,XY/46,YY/47,XYY; Ambiguous Genitalia; Sex Chromosome Mosaicism
Mesh:
Year: 2017 PMID: 29263053
Source DB: PubMed Journal: Ann Clin Lab Sci ISSN: 0091-7370 Impact factor: 1.256