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Genetic mandibulofacial dysostosis was first described by George Andreas Berry in 1889 and formally presented to the London medical community in 1900 by Edward Treacher Collins.
This malady has a several different manifestations and is known by a variety of names. In the USA and Britain, the names Treacher Collins syndrome, Berry's Syndrome, and Berry-Treacher Collins syndrome are used. In Europe it is more likely to be called Franceschetti-Klein syndrome.
I actually have the treacher Collins syndrome, its not all that bad. I don't look terrible, i actually look ok compared to some of the people that have it with me. Im not some moron that hates people with syndromes, theyre not any different. But i hate myself ATM, i don't think i will ever find anybody that will ever think im pretty. People keep telling me looks arent everything, but when you have them, its a lil too east to say.
What else can I help you with?
Is there a treatment for Treacher Collins Syndrome?
No, there is no treatment for Treacher Collins Syndrome.
Who discovered treacher-collins syndrome?
Edward Treacher Collins, an English surgeon and ophthalmologist, is credited with describing Treacher Collins syndrome in 1900. He observed a set of characteristic facial features in affected individuals, which led to the recognition of this genetic disorder.
Do children ever die from Treacher Collins syndrome?
ditto
Can Treacher Collins syndrome be detected before symptoms appear?
No.
What are symptoms of treacher Collins syndrome?
Some symptoms of Treacher Collins syndrome include a small lower jaw, drooping of the lower eyelids, downward slanting eyes, gradual hearing loss and deformed ears.
How many people die from treacher Collins syndrome each year?
19
What are some symptoms of Treacher Collins syndrome?
Some symptoms of Treacher Collins syndrome include a small lower jaw, drooping of the lower eyelids, downward slanting eyes, gradual hearing loss and deformed ears.
What are some syndromes a baby can be born with?
Down Syndrome, Autism, Treacher Collins syndrome, PKU, Fetal Alcohol Syndrome, etc.
What type of people does treacher Collins syndrome affect Is genetic testing available?
Averybody
Is treacher Collins syndrome fatal?
nope its not now stop askin and read a book
How is Treacher Collins syndrome detected?
You can detect Treacher Collins syndrome by looking for the following characteristics:Facial cleft (Tessier 6-7-8 cleft)Hypoplasia of cheeks and mandible bilaterallyColobomas (or congenital scar) of the eyelidsDownward-sloping palpebral fissuresPoorly developed supraorbital rims and cheeksReceding chinMalformation of the earSeverity of Treacher Collins syndrome can vary, but problems faced by children with Treacher Collins syndrome can be quite complicated and require the attention of a professional with experience with these types of patients.
How many children are affected by Treacher Collins syndrome and hemifacial microsomia?
Estimates vary, but approximately 1 in 50,000 children are affected by Treacher Collins syndrome, while hemifacial microsomia occurs in about 1 in 3,500 to 1 in 5,600 live births. Both conditions are considered rare.
