Abandoned by her parents, "Little Monkey" schoolgirl who suffers from Werewolf Syndrome and is covered in hair finds new home

A schoolgirl who was abandoned by her family because she suffers from a rare condition that means her body and face are partially covered in black fur has been adopted.

Liu Jiangli was just two when she was dumped at a nursery school – but carers had to appeal to her family through the local newspapers to come forward after her looks terrified the other children.

The six-year-old was born with a thick coating of black fur on the left side of her face, and there are more patches across 60% of the rest of her body, including inside her left ear.

“It's very itchy,” she told a news agency.

“But it’s not painful.”

Nicknamed the “little monkey”, it is reported that her father never returned to pick her up from the nursery after dropping her off one day, a short time after her mother left the family home.

Eventually, the grandfather of one of her cousins took responsibility for the youngster who has been unable to make friends with other children.

Liu Mingying has looked after the little girl ever since, but worries he won’t be able to afford to pay for her education and that she will always be bullied over her appearance.

The maize farmer admits that he initially felt uncomfortable about the little girl's condition, but now accepts her completely and even jokes about her appetite.

While Liu’s condition has not been officially diagnosed, it is thought that she may be suffering from Hypertrichosis Universalis, otherwise known as Werewolf Syndrome .

http://www.mirror.co.uk/news/weird-news/little-monkey-schoolgirl-who-suffers-868022

Siblings from India don't expect to marry due to 'werewolf syndrome' Heartbreak of three India sisters (via Peter Park)

By RITA DELFINER

THE NEW YORK POST, Thursday, February 9, 2012, p. 25

These three sisters in India have dreams of getting married, but are caught
in a nightmare - each is cursed with an extremely rare genetic disorder
sometimes called "werewolf syndrome."

There are only a few hundred cases in the world of hypertrichosis
universalis, which results in excessive hair over the body and for which
there is yet no cure.

The Raut sisters, Savita, 23, Monisha, 18, and Savitri, 16, of Sangli, a
small village in central India, use a special hair-removal cream, but the
hair grows back quickly on their brow.

"Marriage is not an option for us; it's not likely to happen," Savita was
quoted as saying by the Daily Mail Online. "Who is going to marry us when
hair keeps growing on our faces?"

The girls' mother, Anita Sambhaji Raut, said the trio inherited the
condition from her late husband.

She said when Savita was a baby, she had "little hairs all over her face."

"When I used to take her out as a child, they used to shout 'Here comes the
beast, the witch!' That's what they said."

The girls' mom said that of her six daughters, three have the condition.

Anita was only 12 when she wed her husband in an arranged marriage, and she
did not see him until the day they tied the knot.

"It was only on the day of my marriage that I discovered what he was; [he]
was hairy on his face, ears and body. That's when I found out," she said.

"I was very young. I didn't know what kind of boy he was.

"He scared the hell out of me when he arrived at the [ceremony]."

Savita said that "when I used to go to school, the boys and girls would
shout, 'hairy face,' 'horrible looking,' 'Don't sit next to her,' that's
how they behaved," the paper quoted her as saying.

Her mother said that Savita tries to hold a job, but "they keep her at work
now for 10 to 15 days, and then after that, they ask her to leave as soon
as the hair starts showing through.

"I tell people this is the type of girl she is - hair grows on her face,
she has to apply medicine."

The mom said she would like to get Savita a husband.

"If a good proposal comes in, I'll get her married. If nothing comes in,
she'll have to work and survive. As long as I am living, I have to keep
trying," Anita said.

A documentary filmmaker is planning to tell the sisters' story, which they
hope could help them raise funds for laser surgery to help them get rid of
the unwanted hair, the newspaper said.

In August, BangaloreMirror.com said the sisters were to be treated by
specialists at a hospital in Bangalore, which is getting together a team of
specialists from the United States and Germany to work toward a cure.

The Web site said that only 300 cases of the disorder had been reported
worldwide, and there were only five known cases, including the sisters, in
India.

"These cases are a challenge to the medical fraternity. We hope they find a
cure," said Mansoor Chetlu, coordinator of the New Life Karnataka,
Bangalore Chapter, which is helping the family, according to the site.

rita.delfiner@nypost.com

http://www.nypost.com/p/news/international/werewolf_curse_ja39KCXDRrjK45Qlqk9ODL