Skip navigation

Refine by Type

Results 1 - 10 of 26 for Noonan syndrome 1
  1. Genetics Home Reference: Noonan syndrome From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Noonan syndrome On this page: Description Genetic changes Inheritance Diagnosis ... names Glossary definitions Reviewed March 2011 What is Noonan syndrome? Noonan syndrome is a condition that affects many ...
  2. Noonan syndrome is a disease that can be passed down through families (inherited). It causes abnormal development in many parts of the body. Noonan syndrome used to be called Turner-like syndrome.
  3. Noonan Syndrome (Mayo Foundation for Medical Education and Research)  
  4. ... 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 ...
  5. ... 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 ...
  6. ... to develop RMS as well as other tumors. Noonan syndrome is a condition in which children are short, ...
  7. 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 ...
  8. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  9. 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? ...
  10. Genetic Disorders (National Library of Medicine)  
    Genes are the building blocks of heredity. They are passed from parent to child. They hold DNA, the instructions for making proteins. Proteins do most of the ...
previous · 1 · 2 · 3 · next