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Results 1 - 10 of 11 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. Genetics Home Reference: Cardiomyopathy From the National Institutes of Health (National Library of Medicine)  
    ... Sayre syndrome neutral lipid storage disease with myopathy Noonan syndrome primary carnitine deficiency Salih myopathy You may also search Genetics Home Reference for "Cardiomyopathy" for additional information. Published: April 7, 2014 Lister Hill National Center for Biomedical Communications ...
  3. ... of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their genetic ... cardiofaciocutaneous syndrome. Read more about Costello syndrome and Noonan syndrome . How common is cardiofaciocutaneous syndrome? Cardiofaciocutaneous syndrome is ...
  4. Genetics Home Reference: Costello syndrome From the National Institutes of Health (National Library of Medicine)  
    ... other genetic conditions, cardiofaciocutaneous syndrome (CFC syndrome) and Noonan syndrome. In affected infants, it can be difficult to ... in childhood. Read more about cardiofaciocutaneous syndrome and Noonan syndrome . How common is Costello syndrome? This condition is ...
  5. ... 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 ...
  6. ... 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 ...
  7. Genetics Home Reference: Cherubism From the National Institutes of Health (National Library of Medicine)  
    ... cherubism has been reported in rare cases of Noonan syndrome (a developmental disorder characterized by unusual facial characteristics, ... learning disabilities and cognitive impairment). Read more about Noonan syndrome and fragile X syndrome . How common is cherubism? ...
  8. ... 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 ; ...
  9. 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 ...
  10. ... as: Down syndrome. Fanconi anemia . Neurofibromatosis type 1 . Noonan syndrome . Shwachman-Diamond syndrome . Signs and symptoms of childhood ...
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