Treacher Collins syndrome (TCS) is a rare, genetic craniofacial condition when the bones and tissues of the face do not develop as they should, especially around the cheeks, jaw, and chin.

Treacher Collins syndrome (TCS) is a disorder of craniofacial development and although TCS arises primarily through autosomal dominant mutations in TCOF1, no clear genotype–phenotype correlation ...

Treacher Collins Syndrome. A rare craniofacial disorder, the hallmark of Treacher Collins is the incomplete development of bones in the face, especially the cheekbones, jaw joints and ear canals.

The new movie Wonder, based on the bestselling novel of the same name, follows the emotional ups and downs of the Pullman family as they send their 10-year-old son August off to fifth grade. It ...

Treacher-Collins. The symptoms of this syndrome can affect each child differently because it affects how the bones and tissues inside a child’s face develop. Most people with Treacher-Collins have ...

Heavenli Hill loves English class and digital photography. She especially likes to take photos of nature. She is, in many ways, an average 12-year-old — and she also has Treacher Collins ...

Three distinct genetic mutations have been identified as causing Treacher Collins syndrome (TCS), a rare congenital craniofacial development disorder that affects an estimated 1 in 50,000 live births.

Author with Treacher Collins Syndrome Abandoned as a Baby, Now 'Full of Self Love' Jonathan “Jono” Lancaster has penned a book, Not All Heroes Wear Capes , about his journey By ...

Treacher Collins syndrome is a birth defect that affects the head and face. It can cause physical deformity, hearing problems, and social challenges. There is no cure, but surgery can help.

Michael Rape, a UC Berkeley researcher, with Francis Smith during a Sept. 25 visit to discuss how Rape's research might help others with Smith's craniofacial disorder, Treacher Collins Syndrome.