MASIKINI UGONJWA HUU UNAMTESA MTOTO HUYU KWELI UJAFA UJAUMBIKA.

Ana miaka 8 wezake wamempachika jina la "Fish Boy" kama a.k.a yake lakini jina halilopewa na wazazi wake ni Pan Xianhang amezaliwa katika mji wa Wenling nchini chini akiwa na Ugonjwa wa Ngozi unaojulikana kiutaalam kama LCTHYOSIS neno ili limetoholewa katika neno la kigiriki likimaanisha Samaki.

Ugonjwa huu ukimpata mtu umuathili sana maeneo ya kuzunguka Macho,Pua,Masikio na Mdomo,unasababisha mtu kujikuna sana na kumsababishia mgonjwa maumivu makali sana na hasa nyakati za usiku.

Pan Xianhang was born in Wenling, China with a rare genetic skin disease known as Ichthyosis, after the ancient Greek word for fish.Most sufferers develop dry scaly skin across part of their body, but Pan's case is severe: his scales have affected the shape of his eyes, nose, mouth and ears - and they limit the movement of his arms and legs.

Photoshot / China Foto Press

The condition also means he's in constant pain and struggles to sleep at night because of the itching.
Sufferers are treated with creams, oils and moisturisers, which are designed to hydrate the skin.
Liz Dale a spokesperson for the UK-based Ichthyosis Support Group said: "There is no known cure and treatments for ichthyosis are predominantly keeping the skin moisturised with plenty of emollients i.e. lotions and creams.
"The skin needs to be moisturised to prevent it from further drying out, which could cause the skin to crack, making it more prone to infection, which may be fatal." Last year, Channel 5 documentary The Boy They Call Fish, followed the plight of Vietnamese teenager Minh Anh, who was abandoned as a baby after he was born with a severe form of Ichthyosis.