Results 1 - 10 of 53 for Noonan syndrome 1
  1. Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding ...
  2. Noonan syndrome with multiple lentigines (formerly called LEOPARD syndrome) is a condition that affects many areas of the body. As the condition name suggests, ...
  3. Noonan syndrome is a disease present from birth (congenital) that causes many parts of the body to develop ... Noonan syndrome is linked to defects in several genes. In general, certain proteins involved in growth and development ...
  4. Noonan Syndrome (For Parents) (Nemours Foundation)  
    Congenital Heart Defects/Specifics ... Congenital Heart Defects ... Growth Disorders/Specifics ... Growth Disorders ... noonan, nunan, noonan syndrome, Lymphatic Malformations, ...
  5. Noonan syndrome with multiple lentigines (NSML) is a rare inherited disorder. People with this condition have problems with ... and heart. The genitals may also be affected. Noonan syndrome with multiple lentigines was formerly known as LEOPARD ...
  6. Noonan Syndrome (Mayo Foundation for Medical Education and Research)  
    Genetic Disorders/Specifics ... Genetic Disorders ... Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Mayo Foundation for Medical Education and Research
  7. ... to become cancerous. More than 90 mutations causing Noonan syndrome have been identified in the PTPN11 gene. This ... growth problems, skeletal abnormalities, and other features of Noonan syndrome.Rarely, a person with Noonan syndrome caused by ...
  8. ... the RIT1 gene have been found to cause Noonan syndrome. This condition is characterized by mildly unusual facial ... and many other signs and symptoms. People with Noonan syndrome caused by RIT1 gene mutations often have swelling ...
  9. ... to become cancerous. More than 25 mutations causing Noonan syndrome have been identified in the RAF1 gene. Noonan syndrome is characterized by mildly unusual facial characteristics, short ...
  10. ... proper embryonic development. More than 55 mutations causing Noonan syndrome have been identified in the SOS1 gene. Noonan syndrome is characterized by mildly unusual facial characteristics, short ...
previous · 1 · 2 · 3 · 4 · 5 · 6 · next