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1. my.clevelandclinic.org › health › diseasesTreacher Collins Syndrome: Symptoms, Causes & Treatment

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   Learn about Treacher Collins syndrome, a rare inherited condition that affects facial growth and hearing. Find out how to diagnose, treat and prevent complications with surgery and hearing aids.

2. en.wikipedia.org › wiki › Treacher_Collins_syndromeTreacher Collins syndrome - Wikipedia

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   Treacher Collins syndrome is a genetic disorder that causes facial deformities and hearing loss. Learn about the symptoms, causes, diagnosis, treatment, and prognosis of this rare condition.

3. rarediseases.org › treacher-collins-syndromeTreacher Collins Syndrome | TCS Disease | Symptoms & Treatment

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   Nov 1, 2023 · Treacher Collins syndrome (TCS) is a rare genetic disorder characterized by distinctive features of the head and face. Craniofacial differences tend to involve underdevelopment of the facial skeleton, cheekbones, jaws, palate and mouth which can lead to breathing and feeding difficulties.

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   What is Treacher Collins syndrome?

   • Treacher Collins syndrome is a rare inherited group of conditions that affects the growth of a child’s skull and facial bones. It can cause facial differences and hearing loss. Treatment often includes reconstructive surgery. Without treatment, children with Treacher Collins syndrome can develop complications that require lifelong medical support.

   Treacher Collins Syndrome: Symptoms, Causes & Treatment - Clevelan…

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   What are the symptoms of Treacher Collins syndrome?

   • The most common symptom of Treacher Collins syndrome is underdevelopment of the lower jaw and underdevelopment of the zygomatic bone. This can be accompanied by the tongue being retracted. The small mandible can result in a poor occlusion of the teeth or in more severe cases, trouble breathing or swallowing.

   Treacher Collins syndrome - Wikipedia

   en.wikipedia.org/wiki/Treacher_Collins_syndrome

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   How is Treacher Collins syndrome inherited?

   • Treacher Collins syndrome is inherited in an autosomal-dominant pattern. Mutations in TCOF1, POLR1C, or POLR1D genes can cause Treacher Collins syndrome. TCOF1 gene mutations are the most common cause of the disorder, with POLR1C and POLR1D gene mutations causing an additional 2% of cases.

   Treacher Collins syndrome - Wikipedia

   en.wikipedia.org/wiki/Treacher_Collins_syndrome

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   Can Treacher Collins syndrome be cured?

   • There’s no cure for Treacher Collins syndrome, but healthcare providers have many ways to help. There are surgeries to ease breathing difficulties and hearing loss, as well as surgeries known as craniofacial reconstructions to help correct your child’s facial differences.

   Treacher Collins Syndrome: Symptoms, Causes & Treatment - Clevelan…

   my.clevelandclinic.org/health/diseases/22149-treacher-collins-syndrome

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5. www.chop.edu › treacher-collins-syndromeTreacher Collins Syndrome - Children's Hospital of Philadelphia

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   Learn about the genetic birth defect that causes distinctive facial features and affects the eyes, ears, cheeks, palate and jaw. Find out how CHOP can diagnose, treat and manage the symptoms and complications of Treacher Collins syndrome.

6. medlineplus.gov › treacher-collins-syndromeTreacher Collins syndrome - MedlinePlus

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   Learn about the causes, symptoms, inheritance, and treatment of Treacher Collins syndrome, a genetic disorder that affects facial development. Find out how gene variants in , , and affect ribosomal RNA production and cell survival.

7. www.ncbi.nlm.nih.gov › pmc › articlesTreacher Collins Syndrome: Genetics, Clinical Features and ...

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   Sep 9, 2021 · Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second pharyngeal arches, occurring during fetal development. Features of TCS include microtia with conductive hearing loss, slanting palpebral fissures with possibly coloboma of the lateral part of lower eyelids, midface hypoplasia, micrognathia as ...

8. rarediseases.info.nih.gov › diseases › 9124Treacher-Collins syndrome | About the Disease | GARD

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   Treacher-Collins syndrome is a rare genetic condition that affects the development of facial bones and tissues. Learn about the symptoms, causes, inheritance, and resources for this disease from the Genetic and Rare Diseases Information Center (GARD).