Apert syndrome causes, symptoms, diagnosis & Apert syndrome treatment
Apert syndrome causes, symptoms, diagnosis & Apert syndrome treat…
Oct 18, 2018
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Amelia is diagnosed with a rare genetic syndrome known as Apert syndrome. At birth, her hands and feet were fused together due to a mutation of the tenth chromosome. After a surgery that gave Amelia toes and fingers, she is now learning to grab and open objects. Amelia wants others to know that if you want to be her friend you just have to play nicely together. | Special Books by Special Kids
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30 reactions | Gideon was diagnosed with Apert Syndrome, a genetic disorder characterized by skeletal abnormalities, which can impact a child's ability to breathe, eat and see. Watch Gideon's father as he shares his son's plastic surgery journey. #TrustASPS #PlasticSurgery | American Society of Plastic Surgeons (ASPS) | Facebook
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