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Results 1 - 5 of 5 for Cranioectodermal dysplasia
  1. Cranioectodermal dysplasia 
    Cranioectodermal dysplasia is a disorder that affects many parts of the body. The most common features involve bone ... skull and face are common in people with cranioectodermal dysplasia. Most affected individuals have a prominent forehead (frontal ...
    https://medlineplus.gov/.../condition/cranioectodermal-dysplasia - Genetics
  2. WDR35 gene 
    ... the most commonly mutated gene in people with cranioectodermal dysplasia; at least eight mutations in this gene have ... and skin.The WDR35 gene mutations involved in cranioectodermal dysplasia reduce the amount of functional WDR35 protein. A ...
    https://medlineplus.gov/genetics/gene/wdr35 - Genetics
  3. WDR19 gene 
    ... WDR19 gene have been found in individuals with cranioectodermal dysplasia. This condition is characterized by an elongated head ( ... which include the teeth, hair, nails, and skin. Cranioectodermal dysplasia can also cause a variety of other problems, ...
    https://medlineplus.gov/genetics/gene/wdr19 - Genetics
  4. IFT122 gene 
    ... unclear. Mutations in the IFT122 gene can cause cranioectodermal dysplasia. This condition is characterized by an elongated head ( ... gene mutations have been found in people with cranioectodermal dysplasia. These mutations reduce the amount or function of ...
    https://medlineplus.gov/genetics/gene/ift122 - Genetics
  5. IFT43 gene 
    ... the IFT43 gene is a rare cause of cranioectodermal dysplasia. This condition is characterized by an elongated head ( ... and skin.The IFT43 gene mutation involved in cranioectodermal dysplasia leads to production of an abnormally short IFT43 ...
    https://medlineplus.gov/genetics/gene/ift43 - Genetics