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  2. Treacher Collins syndrome - Wikipedia

    en.wikipedia.org/wiki/Treacher_Collins_syndrome

    Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. [5] The degree to which a person is affected, however, may vary from mild to severe. [5] Complications may include breathing problems, problems seeing, cleft palate, and hearing loss. [5]

  3. Edward Treacher Collins - Wikipedia

    en.wikipedia.org/wiki/Edward_Treacher_Collins

    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

  4. Pierre Robin sequence - Wikipedia

    en.wikipedia.org/wiki/Pierre_Robin_sequence

    Pierre Robin sequence [a] (/ p j ɛər r ɔː ˈ b æ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities.The three main features are micrognathia (abnormally small mandible), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing problems due to obstruction of the upper airway.

  5. Biological mom keeps infant born with rare birth defect after ...

    www.aol.com/news/2016-06-07-biological-mom-keeps...

    But on January 11, when Fisher gave birth, doctor's diagnosed her baby with a rare condition called Treacher Collins syndrome, which is a rare congenital disorder characterized by facial, such as ...

  6. Wonder (film) - Wikipedia

    en.wikipedia.org/wiki/Wonder_(film)

    Wonder. (film) Wonder is a 2017 American coming-of-age family comedy-drama directed by Stephen Chbosky, who co-wrote the screenplay with Steven Conrad and Jack Thorne. It is based on the 2012 novel of the same name by R. J. Palacio and stars Julia Roberts, Owen Wilson, Jacob Tremblay, Mandy Patinkin, and Daveed Diggs.

  7. Hearing loss with craniofacial syndromes - Wikipedia

    en.wikipedia.org/wiki/Hearing_loss_with...

    Researchers have found that most patients with Treacher Collins syndrome have symmetric external ear canal abnormalities and symmetrically dysmorphic or absent ossicles in the middle ear space. Inner ear structure is largely normal. Most patients show a moderate hearing impairment or greater, and the type of loss is generally a conductive ...

  8. Hemifacial microsomia - Wikipedia

    en.wikipedia.org/wiki/Hemifacial_microsomia

    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. If severe, it may result in difficulties in breathing due to obstruction of the trachea ...

  9. Craniofacial cleft - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_cleft

    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. In this case, treatment of mouth anomalies is a part of the treatment of the syndrome.