A peek inside Abbie King’s wardrobe reveals a baby clothes collection to rival Mothercare. Barely contained on the long rail hangs one tiny outfit after the next — a pink fluffy jacket sits next to a spotty green baby dress and a gorgeous white and gold angel outfit bought for a Christmas party.
Doll-sized white cotton socks fill her drawers alongside little jeans and pretty skirts. Many items still have the labels on, ‘0-3 months’, ‘3-6 months’.
A spoilt newborn baby, you may think? Far from it. These clothes, mostly hand-me-downs, have been piling up because Abbie, born 22 months ago, has barely grown to the size of a six-month-old baby.
She suffers from a very rare genetic condition called Russell-Silver syndrome, a form of primordial dwarfism (where the body is smaller than it should be even before birth) which affects only one in 100,000 babies.
Despite being barely 2ft tall and weighing less than 14lb — half what she should at her age — Abbie can walk, laugh, play and throw a tantrum like any normal toddler.
She is a perfectly-formed miniature person — a real-life Thumbelina.
‘When I found out that Abbie wasn’t growing properly, I was terrified she wouldn’t have a normal life,’ says her mother Emma Smith, 29, a former nanny from the Isle of Sheppey, in Kent. ‘But she’s become an independent, cheeky little girl. She gets into all the same trouble as any other toddler, although she probably gets away with more because she’s so gorgeous.’
Back in 2008, she and her partner of 13 years, David King, 33, a farmer and retained firefighter, longed for a girl to complete their family and to be little sister to their son Josh, then three. So they were overjoyed when Emma fell pregnant that summer.
Abbie was delivered by Caesarean section at 38 weeks on February 12, 2009.
‘I would watch my friend’s children grow month after month, while Abbie barely changed. Even now, aged 22 months, she’s only 26in (65cm),’ says Emma.

While Russell-Silver does cause growth defects, children affected by it can live normal lives — unless problems show up at a very young age. Abbie has an average life expectancy and can be treated with growth hormones from the age of four to give her a bit more height. Without these, her adult height wouldn’t be more than 4ft (122cm), but with them there’s a chance she may get to 5ft (152cm).
The physical traits of those affected with Russell-Silver include a large forehead, low-set ears and a small, triangular face.
Looking closely now at Abbie, who is quietly doing a puzzle with her five-year-old brother Josh on the carpet, she does have these features, but it only serves to give her a sweet, elfin quality. Unlike her body, her head has grown at a normal rate so is slightly bigger than the rest of her, which caused her to develop a rather strange way of getting around when she became mobile.
‘She never really crawled, but would scoot around with her head on the floor, bottom stuck up in the air,’ says Emma. ‘When I mentioned it to the doctor, he said it was because her head was the heaviest part of her, so she preferred not to lift it. But she’s happily walking around now.’ (Daily Mail)
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