The patient shown in picture below is having Noonan syndrome.
Noonan syndrome is a disorder that involves unusual facial characteristics, short stature, heart defects present at birth, bleeding problems, developmental delays, and malformations of the bones of the rib cage. Noonan syndrome is caused by changes in one of several autosomal dominant genes.
Noonan syndrome is a type of RASopathy, the underlying mechanism for which involves a problem with a cell signaling pathway.
No cure is known.Treatment is based on symptoms and the underlying problems.
Do you know anyone who is having Noonan syndrome?
What are their symptoms?