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Results 1 - 8 of 8 for Absent skin pigmentation
  1. SNAI2 gene 
    ... of the gene, the snail 2 protein is absent. Lack of snail 2 may disrupt the development of melanocytes in certain areas of the skin, hair, eyes, and inner ear, leading to hearing loss and the patchy loss of pigmentation that are characteristic features of Waardenburg syndrome type ...
    https://medlineplus.gov/genetics/gene/snai2 - Genetics
  2. Pallister-Killian mosaic syndrome 
    ... distinctive facial features, sparse hair, areas of unusual skin coloring (pigmentation), and other birth defects.Most babies with Pallister- ...
    https://medlineplus.gov/.../pallister-killian-mosaic-syndrome - Genetics
  3. Mowat-Wilson syndrome 
    ... condition also affects the eyes, teeth, hands, and skin coloring (pigmentation). Although many different medical issues have been associated ...
    https://medlineplus.gov/genetics/condition/mowat-wilson-syndrome - Genetics
  4. TERC gene 
    ... congenita. This disorder is characterized by changes in skin coloring (pigmentation), white patches inside the mouth (oral leukoplakia), and ...
    https://medlineplus.gov/genetics/gene/terc - Genetics
  5. MSH6 gene 
    ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
    https://medlineplus.gov/genetics/gene/msh6 - Genetics
  6. MSH2 gene 
    ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
    https://medlineplus.gov/genetics/gene/msh2 - Genetics
  7. PMS2 gene 
    ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
    https://medlineplus.gov/genetics/gene/pms2 - Genetics
  8. MLH1 gene 
    ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
    https://medlineplus.gov/genetics/gene/mlh1 - Genetics