اختبار ذكاء عالمي

Eight years Xianhang Pan can not sleep at night.
Known as "Fish Boy" by locals in the eastern Chinese province of Wenling, little Xianhang is covered from head to toe in thick flakes, itchy.
Diagnosed at birth with the rare genetic disease ichthyosis, Pan has lived all his life in excruciating pain, often suffer from overheating and extreme itching.
According to the Argentine daily El Periodico, Pan's mother says the child only wants to attend school without pruritus.
His severe skin alterations have affected the shape of the eyelids, nose, mouth and ears, while limiting the movement of his arms and legs, imagine China reports.
It is estimated that each year more than 16,000 babies are born with some type of ichthyosis, which vary in severity of symptoms, according to the Foundation for Ichthyosis and Related Skin Types.

While there is currently no cure for the disease, cold water can alleviate the symptoms of overheating and a thick cream can help to prevent the skin’s cracking. Doctors are currently looking into other ways to treat the boy.

Pan is not the first to make headlines for this stifling disease.

Metro reports on a 2012 documentary called ‘The Boy They Call Fish’, which highlighted the story of a severely mentally handicapped 18-year-old Vietnamese orphan, Minh Anh, who suffers from the same disease in a special ward of a Saigon hospital.