A 3-year-old girl born with a rare genetic disease often referred to as “brittle bone disease” has won the hearts of thousands across the country with her singing and dancing videos that her mother regularly shares on Facebook.

Topics:  facebook   girl   rare   bone   dancing   disease   
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  • The girl who can’t smile: How a rare disorder became a young woman's ‘greatest gift’
    Tayla Clement, 26, was born with a rare disorder that made it impossible to smile — but she says she is grateful for it. Clement shared her experience with Fox News Digital.
    04/15/2024 - 11:00 pm | View Link
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