Aim. To investigate the cause of infertility in an azoospermic man and to describe the
phenotype of a new 46, XX male case. case report. We present the case of an infertile man …

Background: 46, XX testicular disorder of sexual development is a rare cause of primary
hypogonadism, characterized by a male phenotype despite a female (ie 46, XX) karyotype …

Objective We present a case of XY translocation with male phenotype (46, XX testicular
disorder of sex development) and review the literature. Methods Disorders of sex …

Discussion: We present a clinical case of a male with an XX male syndrome positive for SRY
gene. This is due to a Y to X translocation during meiosis and SRY is the main driver to …

The aim of this study was to characterize the 46, XX testicular disorder, by an adult male
phenotype patient who was diagnosed with the molecular analysis. 46, XX male syndrome …

The aim of this study was to characterize the 46, XX testicular disorder, by an adult male
phenotype patient who was diagnosed with the molecular analysis. 46, XX male syndrome …

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 …

We would like to thank the Contributor for acknowledging the findings of our case report. We
agree with the contributor's recommendation for testosterone replacement therapy to …

The clinical genetics and hormonal status of the 46, XX male is well determined. This is a
rare condition that affects one out 20,000 male births. This study evaluates 5 infertile patients …