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1:18
The Biology Behind Treacher Collins Syndrome | Congenital Syndrome
382 views
1 month ago
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Learn Med in Minutes
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Treacher Collins syndrome explained: key facts for families and fans
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Treacher Collins syndrome (TCS) in infants is a rare genetic disorder that affects the development of facial bones and tissues. #newbornbaby #babylove #cutebaby #prematurebaby #littleangel #NICUbaby #babycare | Yuli Ismalia
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Harold and Niki were born with Treacher Collins syndrome, a rare genetic disorder that affects how facial bones and tissue develop, often causing hearing loss. For years, Harold played football and baseball with a hearing implant placed above the skin, which sometimes glitched with sudden movement. Niki relied on a headband version of the hearing implant that sometimes shifted out of place during cheerleading. In 2025, the two siblings decided together that they were ready for the next step: an
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Facebook
Loma Linda University Children's Health
2:04
Jesse A. Taylor, MD on Instagram: "Treacher Collins Syndrome - In this video, I discuss the comprehensive surgical management of patients with Treacher Collins syndrome including curvilinear mandibular distraction osteogenesis (MDO), orthognathic surgery, and cheek reconstruction utilized at the Children’s Hospital of Philadelphia."
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Treacher Collins syndrome is a rare condition present from birth that mainly affects the shape of the face. It happens in about 1 out of every 50,000 babies and is usually inherited. Children with this condition may have small cheekbones and jaw, slanting eyes, missing or small ears, and hearing problems, but their intelligence is usually normal. The severity can vary from mild to severe, and some babies may have breathing or feeding problems early in life. With proper medical care, surgeries, a
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