The overweight baby that never fills full (photos

Holly Williams, 25, and her daughter Harlow, five, in their Newport home. Harlow was diagnosed with Prader Willi Syndrome when she was just six months old

Holly Williams, 25, and her daughter Harlow, five, in their Newport home. Harlow was diagnosed with Prader Willi Syndrome when she was just six months old

‘In future I will have to take further measures and as Harlow gets older I will more than likely have to get locks for the kitchen.’

As a result of the condition, Harlow – who weighs around 7st – is roughly 44lbs heavier than the average five-year-old girl.

Explaining how this affects their everyday life, Holly continued: ‘She eats a full meal and will say she is hungry again straight away.

Harlow is missing chromosome 15, which controls hunger, and has therefore never experimented what it is like to feel full

Holly and Harlow

Holly and  Harlow

‘It’s really difficult because she constantly wants to eat and I have to make sure she doesn’t.

‘It’s hard to manage and I have to try and explain to her that she’s not really hungry.

‘If I were to leave a plate of cakes on the side and I wasn’t around, Harlow would easily eat them all. It’s happened plenty of times before.

‘She has scoffed an entire grab bag of chocolate that was left on the side before, while I wasn’t in the room.’

Holly says her daughter gets out of breath easily and can't walk far. The mother says she's learning to be 'stern' with Harlow about her snacking

Although Holly does her best to ensure her daughter has a healthy and well-balanced diet she still allows her daughter treats from time-to-time

Aware that her daughter is overweight, Holly says is learning to be stern with Harlow – telling her she can’t have anything else to eat once mealtimes are over.

She continued: ‘I make sure she has a healthy and balanced diet, but she is still allowed treats, as she is just a child after all, so I don’t want to completely deprive her.’

Before having Harlow, Holly didn’t know what Prader-Willi syndrome was – but she says it was evident her daughter wasn’t developing in a usual way very early on.

The mother continued: ‘We knew something was wrong when Harlow was born. She was tiny and only weighed 4lbs 12oz.

‘She was really floppy, had no strength, didn’t cry, and wouldn’t feed properly on a bottle.

‘The doctors assumed it was Prader Willi Syndrome because they said they could tell from her features too, such as her eyes, nose and mouth.’

For the first two weeks of her life, Harlow had to stay in hospital until she began feeding properly and was then officially diagnosed with the condition six months later.

Holly said: ‘She was then really delayed with her milestones.

‘Now she is five, she suffers with some mobility issues. She doesn’t walk far and gets out of breath easily, however, the fact she is overweight doesn’t help.

‘She also suffers with sleep apnoea.’

But despite her condition, Holly says Harlow ‘gets on with life and is a happy girl’ who attends an ordinary primary school.

However, Holly says Harlow has been known to thrown tantrums – especially when her mother says she can’t have more food.

She explained: ‘She will throw her iPad, kick her legs and scream and cry. I have to be stern with her otherwise she would rule my life.

Holly says Harlow will throw tantrums when she's told she can't have anything to eat - including throwing her iPad across the room and crying

Holly says she has a 'really close bond' with her daughter Harlow. The mother-and-daughter recently pictured together

What is Prader-Willi syndrome?

Prader-Willi syndrome is a rare genetic condition that causes problems including constant urges to eat food, restricted growth and reduced muscle tone.

Other potential issues include learning difficulties, lack of sexual development and behavioral problems such as tantrums or stubbornness.

The rare condition, which affects one in every 15,000 children born in England, is caused by a defect on chromosome number 15 – and happens by chance.

Because there is no cure, treatment aims to manage the symptoms – with parents of sufferers urged to get their children to stick to a healthy, balanced diet.

Children with the syndrome can eat up to six times more than children of the same age – and still feel hungry.

It was first described in 1956 by Swiss doctors A Prader, A Labhart and H Willi.

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