Forty-six XX disorder of sex development is an uncommon medical condition observed at
times during the evaluation of a man's fertility. The following is a case series and literature …

OBJECTIVE: To describe and explore the current literature on the rare genetic condition of
46, XX SRY-negative males. In addition, we propose comprehensive clinical guidelines in …

Background 46, XX male syndrome is a rare disorder that usually causes infertility. This
study was established to identify the genetic causes of this condition in a series of 46, XX …

Summary 46, XX male sex reversal syndrome is one of the rarest sex chromosomal
aberrations. The presence of SRY gene on one of the X chromosomes is the most frequent …

Background To review the possible mechanisms proposed to explain the etiology of 46, XX
sex reversal by investigating the clinical characteristics and their relationships with …

Objective To present clinical, chromosomal and hormonal features of ten cases with SRY-
positive 46, XX testicular disorder of sex development who were admitted to our infertility …

The main factor influencing sex determination of an embryo is the sex-determining region Y
(SRY), a master regulatory gene located on the Y chromosome. The presence of SRY …

The 46, XX male syndrome (de la Chapelle syndrome or 46, XX testicular disorder of sex
development) is a rare form of sex reversal with complex mechanisms leading to a large …

BACKGROUND/PURPOSE: XX male is a rare sex chromosomal disorder in infertile men.
The purpose of this study was to distinguish the clinical and genetic features of the 46, XX …

Purpose To investigate the clinical characteristics of different categories of sex-reversed 46,
XX individuals and their relationships with chromosomal karyotype and the SRY gene …