Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 10 for Noonan syndrome 2
  1. Noonan syndrome 
    ... Testing Registry: Noonan syndrome 10 Genetic Testing Registry: Noonan syndrome 2 Genetic Testing Registry: Noonan syndrome 3 Genetic Testing ... Disorders (NORD) ClinicalTrials.gov NOONAN SYNDROME 1; NS1 NOONAN SYNDROME 2; NS2 NOONAN SYNDROME 4; NS4 NOONAN SYNDROME 3; ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. Noonan syndrome with multiple lentigines 
    ... lentigines is very similar to a condition called Noonan syndrome, and it can be difficult to tell the two disorders apart in early childhood. However, the features ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  3. Cardiofaciocutaneous syndrome 
    ... of cardiofaciocutaneous syndrome overlap significantly with those of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  4. Costello syndrome 
    ... of Costello syndrome overlap significantly with those of two other genetic conditions, cardiofaciocutaneous syndrome (CFC syndrome) and Noonan syndrome. In affected infants, it can be difficult ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  5. Neurofibromatosis type 1 
    ... mutations represent the major molecular event underlying ... JM. Neurofibromatosis 1. 1998 Oct 2 [updated 2025 Apr 3]. In: Adam MP, Feldman ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  6. Donnai-Barrow syndrome 
    ... Kantarci S, Ragge NK, Thomas NS, Robinson DO, Noonan KM, Russell MK, Donnai D, Raymond FL, Walsh CA, Donahoe PK, Pober BR. Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy. Am J Med Genet A. 2008 ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics
  7. Critical congenital heart disease 
    ... such as Down syndrome, Turner syndrome, and 22q11.2 deletion syndrome, result from changes in the number or structure of particular chromosomes. Other conditions, including Noonan syndrome and Alagille syndrome, result from mutations in ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  8. 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
  9. 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
  10. 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