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How does treacher collins syndrome affect a person

Ashley Carter, 17, from Taunton in Somerset, was born with Treacher Collins syndrome which affects the development of bones and tissues in the face and was bullied as a child at school.

Treacher Collins syndrome is a condition that affects the development of bones and other tissues of the face. The signs and signs of this disorder differ largely, ranging from nearly unnoticeable to serious. Most influenced persons have underdeveloped facial bones, especially the cheek bones, and a small jaw and chin micrognathia .
Treacher Collins syndrome is an inheritable disorder that causes a baby to be born with distorted facial features. The condition affects bone and soft tissue development in the skull and face, and can lead to abnormally-shaped ears, cheeks, eyelids, and jaws. In severe cases, Treacher Collins syndrome can impair hearing and cause airway ...
Treacher Collins Syndrome Analysis 1617 Words | 7 Pages. Treacher Collins syndrome, a rare congenital syndrome that occurs in only about one out of every fifty-thousand live births (Trainor, Dixon, & Dixon, 2008) can have a significant affects on craniofacial development.
Treacher Collins syndrome An autosomal dominant disorder also known as incomplete mandibulo-facial dysostosis or the Collins-Franceschetti syndrome. It features down-sloping eyes, notches (colobomas) in the eyelids, small mouth and lower jaw, small distorted external ears and often hearing loss.
"People with more severe versions of Treacher Collins syndrome may require several medical procedures and many surgeries" (Paragraph 2) B. "It is about the person below the surface." (Paragraph 4) C. "it breeds ignorance and heartache and leads society to shun those that aren't 'normal.'" (Paragraph 4) D. "but they can still ...
Oct 20, 2021 · Since the earlobe does not contain cartilage it has a large blood supply and may help to warm the ears and maintain balance. However, earlobes...
Treacher Collins syndrome occurs in about one of 10,000 live births. The cause of Treacher Collins syndrome is a genetic mutation that affects the baby's facial development before birth. The affected gene is called TCOF1 and is found on chromosome 5. The mutated gene produces abnormalities in a protein called treacle.
This syndrome is a genetic disorder that mainly affects the bones and tissues in a child's face. It is rare, only affecting about one out of every 50,000 children. Treacher Collins syndrome (TCS) does not affect growth or brain development, but it can cause breathing, hearing, and vision problems. Doctors usually notice the signs of this ...
Treacher Collins Syndrome. This genetic disorder causes underdevelopment or malformation of various parts of the head, including eyes, cheekbones, jaws, mouth, and palate. People with Treacher Collins often experience hearing loss when the inner and/or outer parts of their ears are affected by microtia and/or atresia.
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But unlike most young men, Jono has Treacher Collins syndrome, a genetic disorder that affected the way his facial bones developed while he was in his mother's womb. The condition, which is ...
Oct 07, 2016 · These findings could lead to treatment for people who suffer from limited craniofacial bone growth, such as those affected by a congenital disease known as Treacher Collins Syndrome (TCS).
Treacher Collins syndrome is a genetic birth defect characterized by a range of distinctive craniofacial anomalies that can affect the eyes, ears, cheeks, palate and jaw. A distinctive facial appearance is characteristic of Treacher Collins syndrome. All patients with the disorder share similar observable traits of the disorder, ranging from mild to severe.
Complications Due To Treacher Collin Syndrome. Named after a London ophthalmologist, Edward Treacher Collins, the genetic disorder can cause severe complications. The disorder first described in 1900 has characteristics that can put the affected person's life in danger.
The problems that Treacher Collins syndrome cause for someone is hearing loss and is caused by 3 small bones in the middle ear, which translates sound, and bad development of the ear. People with Collins syndrome normally have regular knowledge. "Scientist think there might be another gene also combined with this syndrome.".
Treacher-Collins syndrome Excerpts from a thought-provoking article at the BBC : At the age of 26, Jono is happy with how he looks, but the genetic disorder that affected the way his facial bones developed in the womb has caused him years of anguish.
The syndrome was named after an ophthalmologist called Edward Treacher Collins in 1900.It can also be known by other names such as Berry-Treacher Collins Syndrome, Franceschetti-Klein Syndrome, Franceschetti-Zwahlen Syndrome and Thomson complex. It is a condition that causes facial malformations and severe hearing loss. Physical Characteristics.
Treacher Collins syndrome (TCS) affects the way the bones of the face develop before a baby is born. This can impact many things, but children with TCS typically have normal intelligence and life expectancy. TCS — also called mandibulofacial dysostosis and Treacher Collins-Franceschetti syndrome — is caused by a genetic mutation (a change ...
Treacher Collins Syndrome is an inherited syndrome that affects the facial structure and features. The characteristics of individuals face with TCS are very distinct. It is very common for people with TCS to have some degree of hearing loss. Theyre nostrel tubes may also be a little narrow. Some