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Results 1 - 9 of 9 for neurofibromatosis
  1. Neurofibromatosis type 2 
    Neurofibromatosis type 2 is a disorder characterized by the growth of noncancerous tumors in the nervous system. The most common tumors associated with neurofibromatosis ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-2 - Genetics
  2. Neurofibromatosis type 1 
    Neurofibromatosis type 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of ... Beginning in early childhood, almost all people with neurofibromatosis type 1 have multiple café-au-lait spots, ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  3. Schwannomatosis 
    ... is usually considered to be a form of neurofibromatosis, which is a group of disorders characterized by ... nervous system. The other two recognized forms of neurofibromatosis are neurofibromatosis type 1 and neurofibromatosis type 2. ...
    https://medlineplus.gov/genetics/condition/schwannomatosis - Genetics
  4. Legius syndrome 
    ... syndrome also occur in a similar disorder called neurofibromatosis type 1. It can be difficult to tell ... of Legius syndrome are similar to those of neurofibromatosis type 1. Mutations in the SPRED1 gene cause ...
    https://medlineplus.gov/genetics/condition/legius-syndrome - Genetics
  5. Constitutional mismatch repair deficiency syndrome 
    ... to those that occur in a condition called neurofibromatosis type 1. These features include changes in skin ... with CMMRD syndrome will develop a feature of neurofibromatosis type 1 called Lisch nodules, which are benign ...
    https://medlineplus.gov/...ional-mismatch-repair-deficiency-syndrome - Genetics
  6. Cherubism 
    ... that causes learning disabilities and cognitive impairment), and neurofibromatosis type 1 (a condition primarily characterized by multiple ... Hagel C, Kohlrusch FK, Wieland I, Zenker M. Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic ...
    https://medlineplus.gov/genetics/condition/cherubism - Genetics
  7. Noonan syndrome with multiple lentigines 
    ... RASopathies include Noonan syndrome, cardiofaciocutaneous syndrome, Costello syndrome, neurofibromatosis type 1, and Legius syndrome. Noonan syndrome with ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  8. Noonan syndrome 
    ... syndrome, the RASopathies include cardiofaciocutaneous syndrome, Costello syndrome, neurofibromatosis type 1, Legius syndrome, and Noonan syndrome with ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  9. Moyamoya disease 
    ... addition to features of another disorder, such as neurofibromatosis type 1, sickle cell disease, or Graves' disease. ...
    https://medlineplus.gov/genetics/condition/moyamoya-disease - Genetics