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Results 1 - 7 of 7 for Noonan syndrome 7
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Noonan syndrome 6 Genetic Testing Registry: Noonan syndrome 7 MedlinePlus Encyclopedia: Noonan Syndrome You might also find information on the ...
  2. ... syndrome also occur in a similar disorder called Noonan syndrome. It can be difficult to tell the two ... disorders differ later in life. Read more about Noonan syndrome . How common is multiple lentigines syndrome? Multiple lentigines ...
  3. ... 35 percent of patients. The genetic cause for Noonan syndrome is a mutation of the PTPN11 gene. Children ... PTPN11 gene mutation may have features associated with Noonan syndrome. These typically include heart malformation, short stature, learning ...
  4. ... or structure of particular chromosomes. Other conditions, including Noonan syndrome and Alagille syndrome, result from mutations in single ... with critical congenital heart disease. Read more about Noonan syndrome ; Turner syndrome ; 22q11.2 deletion syndrome ; Down syndrome ; ...
  5. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... inherited metabolic or congenital muscle disorder such as Noonan syndrome, Pompe disease, fatty acid oxidation defect or Barth ... where a specific chromosome is deleted or duplicated. Noonan syndrome is the most common form associated with pediatric ...
  6. ... as: Down syndrome. Fanconi anemia . Neurofibromatosis type 1 . Noonan syndrome . Shwachman-Diamond syndrome . Signs and symptoms of childhood ...
  7. Congenital Heart Defects and CCHD (March of Dimes Birth Defects Foundation)  
    ... where eggs are stored in a female’s body. Noonan syndrome. This condition prevents normal development in different body ...