Treacher Collins Syndrome - Get information and read articles on Treacher Collins Syndrome sign, symptoms, causes, treatment, prevention and diagnosis at onlymyhealth.com, your complete health guide.
Treacher Collins Syndrome: The TCOF1 gene provides instructions for making a protein called treacle.
Treacher collins syndrome is characterized by the inappropriate development of bones and face tissues. It is a rare condition which affects an estimated 1 in 50,000 people.
Treacher Collins Syndrome is a condition that affects the development of bones and other tissues in the face. Most children with Treacher Collins have normal development and intelligence.
Treacher collins syndrome is characterized by the inappropriate development of bones and face tissues. The signs and symptoms of Treacher Collins Syndrome vary greatly, ranging from almost unnoticeable to severe.
Treacher Collins Syndrome condition has an autosomal dominant pattern of inheritance, which means one copy of the altered gene in each cell is sufficient to cause the disorder.