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Results 1 - 10 of 100 for "Neurofibromatosis," type 1
  1. Neurofibromatosis type 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of tumors along ... Beginning in early childhood, almost all people with neurofibromatosis type 1 have multiple café-au-lait spots, which are ...
  2. ... More than 1,000 NF1 mutations that cause neurofibromatosis type 1 have been identified. Most of these mutations are ... experience fatigue, fever, and easy bleeding or bruising. Neurofibromatosis Type 1 Protein Neurofibromatosis-related protein NF-1 neurofibromin 1 ( ...
  3. Nemours Foundation
  4. Selumetinib is used to treat neurofibromatosis type 1 (NF1; a nervous system disorder that causes tumors to grow on nerves) in children 2 years of age and older who ...
  5. ... syndrome also occur in a similar disorder called neurofibromatosis type 1. It can be difficult to tell the two ... of Legius syndrome are similar to those of neurofibromatosis type 1. Mutations in the SPRED1 gene cause Legius syndrome. ...
  6. ... to those that occur in a condition called neurofibromatosis type 1. These features include changes in skin coloring (pigmentation), ... with CMMRD syndrome will develop a feature of neurofibromatosis type 1 called Lisch nodules, which are benign growths that ...
  7. Neurofibromatosis (National Library of Medicine)  
    ... can become cancerous. There are three types of neurofibromatosis: Type 1 (NF1) causes skin changes and deformed bones. It ...
  8. ... to those that occur in a condition called neurofibromatosis type 1.Individuals with CMMRD syndrome inherit two MSH2 gene ... syndrome.It is thought that the features of neurofibromatosis type 1 in people with CMMRD syndrome are due to ...
  9. ... to those that occur in a condition called neurofibromatosis type 1.Individuals with CMMRD syndrome inherit two MLH1 gene ... syndrome.It is thought that the features of neurofibromatosis type 1 in people with CMMRD syndrome are due to ...
  10. ... to those that occur in a condition called neurofibromatosis type 1.Individuals with CMMRD syndrome inherit two MSH6 gene ... syndrome.It is thought that the features of neurofibromatosis type 1 in people with CMMRD syndrome are due to ...
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