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Results 1 - 10 of 11 for Noonan syndrome 4
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Noonan syndrome 3 Genetic Testing Registry: Noonan syndrome 4 Genetic Testing Registry: Noonan syndrome 5 Genetic Testing Registry: Noonan syndrome 6 ...
  2. ... Genetic Testing Registry - Repository of genetic test information (4 links) PubMed ... syndrome with multiple lentigines progressive cardiomyopathic lentiginosis For ...
  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. 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 ...
  5. 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? ...
  6. Childhood Rhabdomyosarcoma (PDQ): Treatment From the National Institutes of Health (National Cancer Institute)  
    ... type 1 (NF1). Beckwith-Wiedemann syndrome . Costello syndrome . Noonan syndrome . Children who had a high birth weight or ...
  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. ... Turner syndrome , Williams syndrome , Russell-Silver syndrome , and Noonan syndrome Growth hormone deficiency Infections of the developing baby ...
  9. ... as: Down syndrome. Fanconi anemia . Neurofibromatosis type 1 . Noonan syndrome . Shwachman-Diamond syndrome . Signs and symptoms of childhood ...
  10. ... as Down syndrome , neurofibromatosis type 1, Fanconi anemia, Noonan syndrome, and other inherited bone marrow failure syndromes (IBMFS) . ...
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