Results 1 - 10 of 12 for Noonan syndrome 5
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Noonan syndrome 4 Genetic Testing Registry: Noonan syndrome 5 Genetic Testing Registry: Noonan syndrome 6 Genetic Testing Registry: Noonan syndrome 7 ...
  2. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... inherited metabolic or congenital muscle disorder such as Noonan syndrome, ... can be grouped into five categories based on the specific genetic cause of ...
  3. ... of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their genetic ... major feature of cardiofaciocutaneous syndrome. Read more about Noonan syndrome and Costello syndrome . How common is cardiofaciocutaneous syndrome? ...
  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. Cancer in Children and Adolescents From the National Institutes of Health (National Cancer Institute)  
    ... Fraumeni syndrome , Beckwith-Wiedemann syndrome , Fanconi anemia syndrome, Noonan syndrome , and von Hippel-Lindau syndrome , also increase the ...
  6. ... type 1 (NF1). Beckwith-Wiedemann syndrome . Costello syndrome . Noonan syndrome . Children who had a high birth weight or ...
  7. ... type 1 (NF1). Beckwith-Wiedemann syndrome . Costello syndrome . Noonan syndrome . Children who had a high birth weight or ...
  8. ... near the eye during infancy Incontinentia pigmenti syndrome Noonan syndrome Prader-Willi syndrome Retinopathy of prematurity Retinoblastoma Traumatic ...
  9. 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 ...
  10. ... as: Down syndrome. Fanconi anemia . Neurofibromatosis type 1 . Noonan syndrome . Shwachman-Diamond syndrome . Signs and symptoms of childhood ...
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