Mother of baby with rare dwarfism: 'There is nothing wrong with just being different'
Mother of baby with rare dwarfism: 'There is nothing wrong with just …
Oct 30, 2016
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Baby with rare dwarfism goes home after 184 days in hospital
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369K views · 5.1K reactions | Finn, Liam and Alex live with Primordial Dwarfism Type 2, which means they never grow taller than 3 feet. This puts them at risk of developing serious brain conditions such as moyamoya, which consists of blocked arteries at the base of the brain - an area called the basal ganglia. Still, they all live extremely fulfilling lives with certain precautions. From: Britain's Tiniest Toddlers | Real Families | Facebook
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Charlotte, who is five years old, is only two feet and two inches tall and weighs only eight pounds, the equivalent of a newborn baby, due to a genetic disorder known as Primordial Dwarfism. In other words, Charlotte's body is perfectly proportioned but in miniature. Having a family member with special needs can be difficult, but thankfully, this amazing family has found a way to cope and adapt to this special little one! | Discovery Channel Southeast Asia
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