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A baby born with an extremely rare condition has been found with a skull shaped devil horns after a surgical operation to reduce the pressure on his brain.
Clyne Solane, a 22-month-old Filipino baby, was born with a condition called hydranencephaly, which meant that he had a small brain and a skull filled with fluid.
Clyne was operated on in March to relieve the pressure on her brain. However, due to surgery-related complications, parts of her skull collapsed in places where her brain was not formed. The result was a misshapen skull with pronounced ridges that look like devil horns.
Since then, her condition has become more pronounced and now, Clyne must undergo a new surgery at the Filipino Children's Medical Center in Pasig to reconstruct the shape of her skull. Complications of Clyne's condition have had a serious impact on her single mother, 21-year-old Justine Gatarin, who is worried that she will be too weak to survive another operation.
"I do not want to continue with this for the moment because I'm afraid my baby is not strong enough yet, "Gatarin told the Daily Mail.That's why I have trouble making a decision. If we do not, his head will look like this for the rest of his life. "
"Some people say that his head looks like devil horns, but for us there is no doubt that he is an angel. It breaks my heart to see him suffer, "she added.
Hydroanencephaly is an extremely rare condition that develops during pregnancy and prevents the baby's brain from developing completely. It also causes the enlargement of the head. The incurable disease can lead to disability, intellectual problems, convulsions and impaired vision. Clyne already needs help to breathe and needs to be powered by a tube.
The family and friends of Clyne and her mother use social media to raise the money for the medical expenses of the little one. Justine said the family had sold the majority of their property to pay for the surgery, but that her continued medical care was expensive.
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"We sold almost everything we owned to have enough money for the operation. But even after the operation, we must always return regularly to the hospital.," she says.
"The tube in his neck that allows him to breathe must be replaced every six months. I'm sad to see my baby suffer like that. "
Justine says that she hopes Clyne will live as a teenager, as have already made other babies born with this disease. It is rare for people born with hydranencephaly to be born until adulthood. In fact, most die in the womb or in the months following birth. Although the exact causes of hydranencephaly are unknown, it is thought that it is an inherited disorder, according to the National Rare Diseases Organization.
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