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Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. The degree to which a person is affected, however, may vary from mild to severe. Complications may include breathing problems, problems seeing, cleft palate, and hearing loss.
Specialty. Craniofacial surgery, pediatrics. Hemifacial microsomia ( HFM) is a congenital disorder that affects the development of the lower half of the face, most commonly the ears, the mouth and the mandible. It usually occurs on one side of the face, but both sides are sometimes affected.
Some symptoms of CSE, such as depression and sleep issues, can be treated separately, and therapy is available to help patients adjust to any untreatable disabilities. Current treatment for CSE involves treating accompanying psychopathology, symptoms, and preventing further deterioration. History
PRS may occur in isolation, but it is often part of an underlying disorder or syndrome. Disorders associated with PRS include Stickler syndrome, DiGeorge syndrome, fetal alcohol syndrome, Treacher Collins syndrome, and Patau syndrome. Diagnosis. PRS is generally diagnosed clinically shortly after birth.
Treatment of mouth anomalies. There are several options for treatment of mouth anomalies like Tessier cleft number 2-3-7 . These clefts are also seen in various syndromes like Treacher Collins syndrome and hemifacial microsomia, which makes the treatment much more complicated.
Inner ear structure is largely normal. Most patients show a moderate hearing impairment or greater, and the type of loss is generally a conductive hearing loss. Patients with Treacher Collins syndrome exhibit hearing losses similar to those of patients with malformed or missing ossicles (Pron et al., 1993).
Edward Treacher Collins (28 May 1862 – 13 December 1932) was a British surgeon and ophthalmologist. [1] He is best known for describing the Treacher Collins syndrome . Family grave of Edward Treacher Collins in Highgate Cemetery.
Berry published an early description of the rare facial dysostosis condition which was initially called Berry-Treacher Collins syndrome. The English ophthalmologist Edward Treacher Collins gave a fuller description in 1900 and the condition is now generally known as Treacher Collins syndrome.
There are some genetic syndromes, in which hearing loss is one of the known characteristics. Some examples are Down syndrome (aneuploidy), Usher syndrome (autosomal recessive), Treacher Collins syndrome (autosomal dominant), Crouzon syndrome (autosomal dominant), and Alport syndrome (X-linked). [2]
These syndromes include Treacher Collins syndrome and Pierre Robin sequence. Mandibular advancement surgery is one of the modifications needed to improve the airway, others may include reduction of the tongue, tonsillectomy or modified uvulopalatoplasty .