female testicular syndrome
XX male syndrome also known as de la Chapelle syndrome is a rare congenital intersex condition in which an individual with a 46 XX karyotype otherwise associated with females has phenotypically male characteristics that can vary among cases. Assisted Reproductive Techniques and Pregnancy Results in Women with Mayer-Rokitansky-Küster-Hauser Syndrome Undergoing Uterus Transplantation.
Note Ovarian Artery Directly From Aorta Similarly Testicular Artery Atlas De Anatomia Anatomia Obstetricia
Journal of Pediatric and Adolescent Gynecology Vol33 No4 p410-414.
. The Czech Experience Chmel et al. Synonyms include 46XX testicular difference of sex development 46XX DSD 46XX sex reversal nonsyndromic 46XX.
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