Abstract 46, XX testicular disorder of sex development is a rare syndrome characterized by
an inconsistency between genotype and phenotype. Affected individuals present variant …

Background 46, XX testicular disorder of sex development is a rare genetic syndrome,
characterized by a complete or partial mismatch between genetic sex and phenotypic sex …

In this case report, we present the case of a 31-year-old man who presented with primary
infertility, azoospermia and occasional sexual dysfunction. History and general physical …

Abstract 46, XX male sex reversal syndrome is a rare genetic cause of male infertility. We
report on two new cases of this syndrome in men presenting with hypogonadism and …

Background: 46 XX male syndrome, a rare case of infertility was first reported by de la
Chapelle in 1964. In newborn males, the incidence rate of the syndrome varies from 1/9000 …

Purpose: To identify the clinical characteristics of SRY-negative male patients and genes
related to male sex reversal, we performed a retrospective study using cases of 46, XX …

The 46, XX male syndrome is a very rare disorder/difference of sex development (DSD).
Characterized by a 46, XX karyotype with a male phenotype and various abnormalities …

Background: 46 XX testicular disorder of sex development (DSD) is rare disorder with
incidence of 1; 20,000 in new-born males. Majority of cases occur due tothe translocation of …

Conclusion: The 46, XX testicular DSD is a rare form of sex reversal with complex
mechanisms leading to a large spectrum of clinical manifestations ranging from ambiguous …

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 …