The risk of a gonadal tumor is high in testicular disorder of sexual development (DSD) with
the Y chromosome, but cases of DSD without the Y chromosome are extremely rare. We …

The 46, XX testicular disorder of sex development (46, XX testicular DSD) is a rare
phenotype associated with disorder of the sex chromosomes. We describe the clinical …

OBJECTIVE: To describe a 46, XX male whose infertility is not accounted for by a
translocation of the SRY gene to the X chromosome or to the autosomes. DESIGN: Case …

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 …

The presence of Y chromosome material in patients with disorders of sex development
(DSD) has been associated with a high risk of gonadoblastoma. Therefore, gonadectomy is …

Abstract 46 XY gonadal dysgenesis patients often develop gonadal tumors, including
gonadoblastoma and other types of germ cell tumors. We report a case of a 16-year-old …

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 objective of this study was to examine risks for gonadal malignancy in a large sample of
adult female patients with disorders of sex development (DSD). A retrospective …

Ovotesticular DSD is not an uncommon disorder. The presence of Y chromosome confers a
high risk of neoplastic transformation in dysgenetic gonads. The neoplastic development in …

Objective Phenotypic female disorders of sex development (DSD) patients with Y
chromosome or Y‐derived sequence have an increased risk of gonadal germ cell tumours …