A two-year-old boy is mistaken for a doll because of a rare condition that causes his skin to shed every day.

Michal Winter, from Derby, suffers from harlequin ichthyosis (HI) which caused him to be born with thick scales of skin.

Shocking pictures of Michal while he was in hospital show how his tight skin caused his eyelids and lips to turn inside out.

Doctors diagnosed him with HI and warned he could die within the first few weeks of life because he was vulnerable to catching infections.

Michal pulled through. But without constant care, his skin cracks and leaves him red-raw. His mother Anna Ciesielska has to moisturise him every four hours.

The condition can make it hard for him to move without his skin cracking, and it also means he has to be kept out of the sun because he can burn easily.

Strangers mock Michal’s appearance online and passers-by are shocked to discover he is a ‘real boy’, said Ms Ciesielska, 30.

Michal Winter, two, (pictured) is mistaken for a doll because of a rare condition called Harlequin ichthyosis that causes his skin the shed every day

Babies with the condition are covered in thick plate-like scales of skin. The tightness of the skin pulls around the eyes and the mouth, forcing the eyelids and lips to turn inside out (pictured, Michal at birth)

Mother, Anna Ciesielska, 30, says strangers are cruel about her son

Ms Ciesielska was kept from her baby for hours while doctors tried to work out what was wrong with Michal

Ms Ciesielska, from Derby, said: ‘People will come up to me and ask what happened to him and if they can help.

‘I was in a shop and someone came up to us and was staring at Michal and asked if he was a doll.

‘When Michal moved he was totally surprised, they were surprised he was a real boy.

‘When we go out people stare at us, their jaws drop. Sometimes a person will see a photo of him online and message me saying he looks like a doll, it really upsets me.

‘Michal is a perfectly normal boy with a wonderful nature. He just has this skin condition.’

Ms Ciesielska, who cares for Michal full-time, found out Michal had HI after he was born covered in plates of thick, cracked skin.

Doctors were initially baffled and had to keep Michal from his mother for hours while they ran tests.

Ms Ciesielska says passers-by come up to her thinking she’s pushing a doll in her pram

Ms Ciesielska says people are surprised when Michal moves and shows them he is a real boy

Ms Ciesielska applies two different types of cream to Michal every four hours to ensure his skin is constantly protected and moisturised. Pictured together at home in Derby

Ms Ciesielska said: ‘I didn’t see him initially when he was born, only a few hours later. When I first saw him I was obviously very upset.

‘I was worried that he would suffer and was in pain. Eventually, one of the doctors broke the news to me about what had happened.’

Medics told Ms Ciesielska her son may not survive because babies with the condition experience dehydration more often and develop life-threatening infections.

HI patients lose the barrier between their body and the environment, and therefore are unable to control fluid loss, fight infections and regulate their temperature.

The genetic condition can also inhibit growth, which has made Michal smaller than others his age.

Ms Ciesielska said: ‘It was a huge shock. I thought I was going to have a healthy baby. Not even the doctors at first knew what was wrong with him.

Michal is smaller than others his age because his condition inhibits growth

Ms Ciesielska said she has to keep Michal away from direct sunlight because it can burn his skin. He also gets cold very easily because he can’t regulate his temperature

Ms Ciesielska said she was devastated when she was told about Michal’s condition. Doctors said Michal may not survive because newborns are at risk of infections and dehydration