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Results 1 - 10 of 49 for "Noonan's%syndrome"
  1. Noonan syndrome 
    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 ...
    https://medlineplus.gov/ency/article/001656.htm - Medical Encyclopedia
  2. Noonan syndrome with multiple lentigines 
    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 ...
    https://medlineplus.gov/ency/article/001473.htm - Medical Encyclopedia
  3. Noonan syndrome 
    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 ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  4. Noonan syndrome with multiple lentigines 
    Noonan syndrome with multiple lentigines (formerly called LEOPARD syndrome) is a condition that affects many areas of the body. As the condition name suggests, ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  5. 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
    https://www.mayoclinic.org/.../symptoms-causes/syc-20354422?p=1 - External Health Links
  6. Noonan Syndrome (For Parents) (Nemours Foundation)  
    Congenital Heart Defects/Specifics ... Congenital Heart Defects ... Growth Disorders/Specifics ... Growth Disorders ... Nemours Foundation
    https://kidshealth.org/en/parents/noonan-syndrome.html - External Health Links
  7. PTPN11 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  8. 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 ...
    https://medlineplus.gov/geneticdisorders.html - Health Topics
  9. Congenital Heart Defects (National Library of Medicine)  
    What are congenital heart defects? Congenital heart defects (CHDs) are problems with the structure of the heart. "Congenital" means that that the problems ...
    https://medlineplus.gov/congenitalheartdefects.html - Health Topics
  10. 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 ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
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