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Results 1 - 7 of 7 for Cafe au lait "spots," multiple
  1. Neurofibromatosis type 1 
    ... almost all people with neurofibromatosis type 1 have multiple café-au-lait spots, which are flat patches on the skin that ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  2. Legius syndrome 
    ... skin coloring (pigmentation). Almost all affected individuals have multiple café-au-lait spots, which are flat patches on the skin that ...
    https://medlineplus.gov/genetics/condition/legius-syndrome - Genetics
  3. SPRED1 gene 
    ... gene cause Legius syndrome, a condition characterized by multiple café-au-lait spots, which are flat patches on the skin that ...
    https://medlineplus.gov/genetics/gene/spred1 - Genetics
  4. Noonan syndrome with multiple lentigines 
    ... brown skin spots called café-au-lait spots. Café-au-lait spots tend to develop before the lentigines, appearing within the first year of life in most affected people.Of the people with Noonan syndrome with multiple lentigines who have heart defects, about 80 percent ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  5. Neurofibromatosis-1 
    ... the same NF1 gene change. "Coffee-with-milk" ( café au lait ) spots are the hallmark symptom of NF1. Many healthy people have one or two small café au lait spots. However, adults who have six or more spots ...
    https://medlineplus.gov/ency/article/000847.htm - Medical Encyclopedia
  6. Skin Pigmentation Disorders (National Library of Medicine)  
    Pigmentation means coloring. Skin pigmentation disorders affect the color of your skin. Your skin gets its color from a pigment called melanin. Special cells in the ...
    https://medlineplus.gov/skinpigmentationdisorders.html - Health Topics
  7. Constitutional mismatch repair deficiency syndrome 
    ... skin that are darker than the surrounding area (café-au-lait spots). Some affected individuals have freckling or patches of ...
    https://medlineplus.gov/...ional-mismatch-repair-deficiency-syndrome - Genetics