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Results 1 - 9 of 9 for Noonan syndrome 6
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Noonan syndrome 5 Genetic Testing Registry: Noonan syndrome 6 Genetic Testing Registry: Noonan syndrome 7 MedlinePlus Encyclopedia: ...
  2. 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 ...
  3. ... 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 ...
  4. ... 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 ...
  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. ... near the eye during infancy Incontinentia pigmenti syndrome Noonan syndrome Prader-Willi syndrome Retinopathy of prematurity Retinoblastoma Traumatic ...
  7. What's Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... such as fatty acid oxidation, Barth syndrome, or Noonan syndrome. Cardiomyopathy can also be a consequence of another ...
  8. ... as Down syndrome , neurofibromatosis type 1, Fanconi anemia, Noonan syndrome, and other inherited bone marrow failure syndromes (IBMFS) . ... inherited conditions such as preleukemia (also called myelodysplastic syndrome ... was diagnosed with leukemia before age 6 has a 20% to 25% chance of developing ...
  9. 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 ...