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  2. Coloboma - Wikipedia

    en.wikipedia.org/wiki/Coloboma

    Treacher Collins syndrome, autosomal dominant syndrome caused by mutation of TCOF1. Coloboma is part of a set of characteristic facies that features craniofacial malformations, such as downslanting eyes, ear anomalies, or hypoplasia of zygomatic bone and jaw (micrognathia).

  3. Treacle protein - Wikipedia

    en.wikipedia.org/wiki/Treacle_protein

    Mutations in this gene have been associated with Treacher Collins syndrome, a disorder which includes abnormal craniofacial development. Alternate transcriptional splice variants encoding different isoforms have been found for this gene, but only three of them have been characterized to date.

  4. First arch syndrome - Wikipedia

    en.wikipedia.org/wiki/First_arch_syndrome

    Examples of first arch syndromes include Treacher Collins syndrome and Pierre Robin syndrome. References This page was last edited on 30 October 2023, at 02:53 ...

  5. Alison Midstokke - Wikipedia

    en.wikipedia.org/wiki/Alison_Midstokke

    Midstokke was born with Treacher Collins syndrome, a congenital condition which affects the development of the face. In addition to her acting work, she has worked as a model with different artists and photographers, and has served on the boards of various organizations for people with facial differences. References

  6. 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.

  7. Ribosomopathy - Wikipedia

    en.wikipedia.org/wiki/Ribosomopathy

    Abnormal ribosome biogenesis is linked to several human genetic diseases. [citation needed]Ribosomopathy has been linked to skeletal muscle atrophy, [11] and underpins most Diamond–Blackfan anemia (DBA), [2] the X-linked subtype of dyskeratosis congenita (DKCX), [12] [13] Treacher Collins syndrome (TCS), [2] [14] Shwachman–Diamond syndrome (SDS) [15] and 5q-myelodysplastic syndrome.(5q ...

  8. Hunter syndrome - Wikipedia

    en.wikipedia.org/wiki/Hunter_syndrome

    Hunter syndrome is caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). [2] [3] The lack of this enzyme causes heparan sulfate and dermatan sulfate to accumulate in all body tissues. [4] Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. [4] The symptoms of Hunter syndrome are comparable ...

  9. Hearing loss with craniofacial syndromes - Wikipedia

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

    Individuals with Treacher Collins syndrome often have both cleft palate and hearing loss, in addition to other disabilities. Hearing loss is often secondary to absent, small or unusually formed ears and commonly results from malformations of the middle ear.