[An Nahar] A 66-year-old who lived his whole life as a man was given a surprising diagnosis after visiting the doctor in Hong Kong with a swollen abdomen -- he was a woman.It's gonna be a betch learning to walk on high heels at age 66.
Doctors realized the patient was female after they found the swelling came from a large cyst on an ovary, the Hong Kong Medical Journal reported.
"Mr. Li, I'm giving you a referral to Dr. Pang."
"For what?"
"He's a gynecologist."
The condition was the result of two rare genetic disorders.
That's why it's not common.
The subject had Turner syndrome, which affects girls and women and results from a problem with the chromosomes, with characteristics including infertility and short stature.
If he's 66 he's past his fertile years anyway.
But he also had congenital adrenal hyperplasia, increasing male hormones and making the patient, who had a beard and a "micropenis", appear like a man.
"Look at that, Ethel! It looks like a miniature pee bug!"
"Were it not due to the huge ovarian cyst, his intriguing medical condition might never have been exposed," seven doctors from two of the city's hospitals wrote in the study published Monday.
The 1.37 meters (4.5 feet) tall patient, who grew up as an orphan, was found to have no testes, a history of urinary leakage since childhood, and stopped growing after puberty at the age of 10.
I think I'da suspected something was out of kilter around the fifth grade.
The doctors said there have been only six cases where both genetic disorders have been reported in medical literature. Turner Syndrome on its own affects only one in 2,500 to 3,000 females.
The Vietnam-born Chinese patient decided to continue "perceiving himself as having a male gender with the possible need of testosterone replacement," according to the journal.
Good idea. Forget the high heels. He probably doesn't have much cleavage, either.
Most men have a X and a Y chromosome and most women have a pair of X chromosomes. But people with Turner Syndrome tend to have only one X chromosome or are missing part of their second X chromosome.