Skip navigation

Refine by Type

Results 1 - 9 of 9 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. ... 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. 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 ...
  5. ... near the eye during infancy Incontinentia pigmenti syndrome Noonan syndrome Prader-Willi syndrome Retinopathy of prematurity Retinoblastoma Traumatic ...
  6. 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 ...
  7. ... Turner syndrome , Williams syndrome , Russell-Silver syndrome , and Noonan syndrome Growth hormone deficiency Infections of the developing baby ...
  8. ... as: Down syndrome. Fanconi anemia . Neurofibromatosis type 1 . Noonan syndrome . Shwachman-Diamond syndrome . Signs and symptoms of childhood ...
  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 ...