featured-image

The youngster also has pulmonary stenosis and in October 2023, his mum Michaela King was informed that he needed open heart surgery. Our community members are treated to special offers, promotions and adverts from us and our partners. You can check out at any time.

More info A Scots tot has been given a 50 per cent chance of survival after getting diagnosed with a rare genetic disorder that requires heart surgery. Rupert King from Edinburgh was born with Noonan syndrome, a genetic disorder which can cause a wide range of distinctive features and health problems. The youngster also has pulmonary stenosis and in October 2023, his mum Michaela King was informed that he needed open heart surgery.



The family will travel to Great Ormond Street Hospital in London for surgery next week. Still, Michaela says Rupert has only been given a 50 per cent chance of surviving the procedure and will have a greater chance of developing a stroke or brain damage. The 32-year-old is terrified of her wee one going into surgery and has wanted to be a mum since she was just 15.

According to the NHS, Noonan syndrome is present from before birth, although milder cases may not be diagnosed until a child gets older. The most common features are unusual facial features such as a broad forehead, drooping eyelids and a wider-than-usual distance between the eyes. It's estimated that between 1 in 1,000 and 1 in 2,500 children are born with Noonan syndrome.

It affects both sexes and all ethnic groups equally. .

Back to Beauty Page