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Results 1 - 9 of 9 for Noonan syndrome 3
  1. Noonan syndrome 
    ... Testing Registry: Noonan syndrome 2 Genetic Testing Registry: Noonan syndrome 3 Genetic Testing Registry: Noonan syndrome 4 Genetic Testing ... NOONAN SYNDROME 2; NS2 NOONAN SYNDROME 4; NS4 NOONAN SYNDROME 3; NS3 NOONAN SYNDROME 5; NS5 NOONAN SYNDROME 8; ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. Cardiofaciocutaneous syndrome 
    ... of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their genetic cause and ... Genet A. 2006 Aug 1;140(15):1681-3. doi: 10.1002/ajmg.a.31315. No abstract ... T, Neri G. The cardiofaciocutaneous syndrome. J Med Genet. 2006 Nov;43(11):833- ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  3. Noonan syndrome with multiple lentigines 
    ... Registry: LEOPARD syndrome 2 Genetic Testing Registry: LEOPARD syndrome 3 Genetic Testing Registry: Noonan syndrome with multiple lentigines Noonan syndrome with multiple ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  4. Costello syndrome 
    ... other genetic conditions, cardiofaciocutaneous syndrome (CFC syndrome) and Noonan syndrome. In affected infants, it can be difficult to tell the three conditions apart based on their physical features. However, ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  5. 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
  6. 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
  7. Cherubism 
    ... growths have been reported in rare cases of Noonan syndrome (a developmental disorder characterized by unusual facial characteristics, ... Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case ... Vivo. 2021 May-Jun;35(3):1711-1736. doi: 10.21873/invivo.12431. Citation ...
    https://medlineplus.gov/genetics/condition/cherubism - Genetics
  8. 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
  9. 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 ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics