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Results 1 - 10 of 10 for Noonan syndrome 1
  1. Noonan syndrome 
    Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. Noonan syndrome with multiple lentigines 
    Noonan syndrome with multiple lentigines (formerly called LEOPARD syndrome) is a condition that affects many areas of the body. As the condition name suggests, ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  3. Cardiofaciocutaneous syndrome 
    ... of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their genetic ... affected individuals may actually have Costello syndrome or Noonan syndrome, which are also caused by variants in genes ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  4. Neurofibromatosis type 1 
    ... in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS). Am J Med Genet A. 2003 May ... mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome. Am J Hum Genet. 2005 Dec;77(6): ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  5. Costello syndrome 
    ... other genetic conditions, cardiofaciocutaneous syndrome (CFC syndrome) and Noonan syndrome. In affected infants, it can be difficult to ... These individuals may actually have CFC syndrome or Noonan syndrome, which are caused by variants in related genes. ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  6. Baraitser-Winter syndrome 
    ... hypertelorism, and mental retardation: Baraitser-Winter syndrome or Noonan syndrome? J Med Genet. 1993 May;30(5):425- ...
    https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome - Genetics
  7. Factor XI deficiency 
    ... 25 percent of people with another disorder called Noonan syndrome have factor XI deficiency. F11 Severe factor XI ...
    https://medlineplus.gov/genetics/condition/factor-xi-deficiency - Genetics
  8. Cherubism 
    ... growths have been reported in rare cases of Noonan syndrome (a developmental disorder characterized by unusual facial characteristics, ...
    https://medlineplus.gov/genetics/condition/cherubism - Genetics
  9. Critical congenital heart disease 
    ... or structure of particular chromosomes. Other conditions, including Noonan syndrome and Alagille syndrome, result from mutations in single ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  10. Donnai-Barrow syndrome 
    ... 0883073807301933. Citation on PubMed Pober BR, Longoni M, Noonan KM. A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: clinical features and differential diagnosis. Birth Defects Res A Clin Mol Teratol. 2009 Jan;85(1):76-81. doi: 10.1002/bdra.20534. Citation ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics