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Results 1 - 10 of 17 for Noonan syndrome 3
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Noonan syndrome 2 Genetic Testing Registry: Noonan syndrome 3 Genetic Testing Registry: Noonan syndrome 4 Genetic Testing Registry: Noonan syndrome 5 ...
  2. ... of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their genetic cause and specific patterns of signs and symptoms; however, it can be difficult to tell these ... is cardiofaciocutaneous syndrome? Cardiofaciocutaneous syndrome ...
  3. 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 tell the three conditions apart based on their physical features. However, ...
  4. Cancer in Children and Adolescents From the National Institutes of Health (National Cancer Institute)  
    ... RB1 ( 7 ). However, retinoblastoma accounts for only about 3 percent of all cancers in children. Inherited mutations associated with certain familial syndromes, such as Li-Fraumeni syndrome , Beckwith-Wiedemann syndrome , Fanconi anemia syndrome, Noonan syndrome , and von Hippel-Lindau syndrome , also increase ...
  5. ... links) PubMed - Recent literature OMIM - Genetic disorder catalog (3 ... syndrome with multiple lentigines progressive cardiomyopathic lentiginosis For ...
  6. ... 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 ...
  7. ... to develop RMS as well as other tumors. Noonan syndrome is a condition in which children are short, ...
  8. 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 ...
  9. ... or structure of particular chromosomes. Other conditions, including Noonan syndrome and Alagille syndrome, result from mutations in single ... with critical congenital heart disease. Read more about Noonan syndrome ; Turner syndrome ; 22q11.2 deletion syndrome ; Down syndrome ; ...
  10. Genetic Disorders (National Library of Medicine)  
    ... can also happen during your lifetime. There are three types of genetic ... Down syndrome is a chromosomal disorder. Complex disorders, where there ...
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