Literature DB >> 29263053

A Novel Sex Chromosome Mosaicism 45,X/45,Y/46,XY/46,YY/47,XYY Causing Ambiguous Genitalia.

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.
© 2017 by the Association of Clinical Scientists, Inc.

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


  1 in total

1.  Successful surgical sperm retrieval from a patient with 45,X/46,XY mosaicism followed by in vitro fertilization pregnancy: A case report.

Authors:  Yu Zhang; Zheng Liu; Jian Ou; Ling-Xiao Zhang; Wei-Ying Lu; Qi Li; Yanlin Ma
Journal:  Medicine (Baltimore)       Date:  2020-10-02       Impact factor: 1.817

  1 in total

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