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Results 1 - 6 of 6 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
  6. Bone Diseases (National Library of Medicine)  
    Your bones help you move, give you shape and support your body. They are living tissues that rebuild constantly throughout your life. During childhood and ...
    https://medlineplus.gov/bonediseases.html - Health Topics