
Marked by craniofacial deformities, Treacher Collins syndrome is a rare genetic disorder. Some of its symptoms include conductive hearing loss, small lower jaw or micrognathia and downward slanting eyes. In addition, patients may also experience malformed ears, drooping lower eyelids as well as underdeveloped zygoma. In addition to its symptoms, causes, and treatments, there are other interesting things to know about this disease including who discovered Treacher Collins syndrome.
The Discovery of Treacher Collins Syndrome
Who discovered Treacher Collins syndrome? An English surgeon named Edward Treacher Collins discovered this medical condition in 1900. During that time, he was able to describe the essential traits of the disease. He was also an ophthalmologist. One of his widely recognized works was entitled “Researches into the Anatomy and Pathology of the Eye,” which was released in 1896. The prevalence of this condition is one in every 10,000 births.
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