XX maleness is a rare syndrome with a frequency of 1 in 20 000–25 000 males. XX males
exist in different clinical categories with ambiguous genitalia or partially to fully mature male …

Background Male sex reversal syndrome is a rare genetic cause of male infertility with an
overall incidence of 1/20,000–1/100,000 males. There is mismatching between the genetic …

Background: Systemic sclerosis may affect male and female fertility. Premature ovarian
failure has been reported in female systemic sclerosis patients, but the effects on male …

Individuals with male phenotypes and 46 XX karyotype appear in about 1 of 20,000 births
with clinical features varying from normal male appearance to sexual ambiguity and …

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 …

The sex-determining region Y (SRY) gene is responsible for the initial sex-determining
switch in the developing human embryo, causing the primitive gonad in a normal XY …

46, XX male (de la Chapelle syndrome) is a rare syndrome with a frequency of 1 in 20,000–
25,000 males. 46, XX males exist in different clinical categories with ambiguous genitalia or …

Male pseudohermaphroditism (MPH) is the abnormal development of genitalia in an
individual with a 46, XY chromosome complement and testicular tissue. The etiology of MPH …

We report a 46 XX male syndrome diagnosed after failure of gonadotropin therapy taken for
hypogonadotropic hypogonadism due to a pituitary macroadenoma. A 39-year-old man with …

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 …