Abstract 47, XYY syndrome is a sex chromosomal anomaly in men, which may be
associated with infertility and has an incidence of 0.1% of male births. The clinical and …

An individual's sexual phenotype is usually determined by the presence or absence of the Y
chromosome in the embryo's karyotype, however, due to abnormal X/Y terminal exchange …

AccordingtoDSM-IV-TR, genderidentitydisorder (GID)(also known as transsexualism) has
two features: a strong and persistent cross-gender identification and persistent discomfort …

STUDY QUESTION Which is the prevalence of a 47, XXY karyotype in human blastocysts
biopsied during preimplantation genetic testing for aneuploidies (PGT-A) cycles …

Objective To describe the gonadal features of patients with 45, X/46, XY mosaicism, and to
evaluate the prevalence of gonadal tumor in different phenotypes. Materials and Methods …

Abstract Background: The 45, X/46, XY karyotype has been associated with mixed gonadal
dysgenesis (MGD) and ovotesticular disorder of sex development (DSD). Our aim was to …

Ovotesticular disorder of sex development is historically thought to confer a relatively low
risk of germ cell malignancy relative to other disorders of sex development. This is likely due …

Background Males with a 47, XXY karyotype have the clinical phenotype of Klinefelter
syndrome. A few 47, XXY cases with a female phenotype have been reported. These …

Context Larger studies on outcomes in males with 45, X/46, XY mosaicism are rare.
Objective To compare health outcomes in males with 45, X/46, XY diagnosed as a result of …

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 …