Noonan Syndrome (NS) is an autosomal dominant RASopathy. It is characterized by facial dysmorphism, short stature and congenital heart defects1 . In addition, circumscribed lymphangioma is a known, but rare… Click to show full abstract
Noonan Syndrome (NS) is an autosomal dominant RASopathy. It is characterized by facial dysmorphism, short stature and congenital heart defects1 . In addition, circumscribed lymphangioma is a known, but rare manifestation of NS.
               
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