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Results 1 - 10 of 21 for Noonan syndrome 2
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Noonan syndrome 1 Genetic Testing Registry: Noonan syndrome 2 Genetic Testing Registry: Noonan syndrome 3 Genetic Testing Registry: Noonan syndrome 4 ...
  2. ... with critical congenital heart disease. Read more about Noonan syndrome ; Turner syndrome ; 22q11.2 deletion syndrome ; Down syndrome ; Alagille syndrome ; and phenylketonuria . ...
  3. ... syndrome also occur in a similar disorder called Noonan syndrome. It can be difficult to tell the two disorders apart in early childhood. However, the features ...
  4. ... of cardiofaciocutaneous syndrome overlap significantly with those of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their ...
  5. Genetics Home Reference: Costello syndrome From the National Institutes of Health (National Library of Medicine)  
    ... 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 ...
  6. ... a less favorable outcome include • Age less than 2 years • Low platelet count • Elevated hemoglobin F levels. There have been a few cases of children under the age of 1 year with Noonan syndrome and a PTPN11 gene mutation where the disease ...
  7. ... old. In JMML, too many myelocytes and monocytes (two types of WBCs) are produced from ... type 1 and Noonan syndrome — can make a child more likely to develop ...
  8. 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? ...
  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. Genetic Disorders (National Library of Medicine)  
    ... are the structures that hold our genes. Down syndrome is a chromosomal disorder. Complex disorders, where there are mutations in two or more genes. Often your lifestyle and environment ...
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