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Results 1 - 10 of 29 for Noonan syndrome 1
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... gov Research studies OMIM Genetic disorder catalog Conditions > Noonan syndrome On this page: Description Genetic changes Inheritance Diagnosis ... names Glossary definitions Reviewed March 2011 What is Noonan syndrome? Noonan syndrome is a condition that affects many ...
  2. Noonan syndrome is a disease that can be passed down through families (inherited). It causes many parts of ... Noonan syndrome is linked to defects in several genes. Certain proteins involved in growth and development become overactive ...
  3. Noonan Syndrome (Mayo Foundation for Medical Education and Research)  
  4. ... 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 ...
  5. 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 ...
  6. ... 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 ...
  7. ... 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 ...
  8. 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 ...
  9. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  10. ... 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 ; ...
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