Coronary arteriopathy in a patient with Noonan phenotype: Case report

• Main Authors: Simran Jain (Author), M. S. Ravindra (Author), Yogesh Chintaman Sathe (Author), Snehal M. Kulkarni (Author), Ashish Banpurkar (Author)
• Format: Book
• Published: Wolters Kluwer Medknow Publications, 2024-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Noonan syndrome (NS) is a pleomorphic genetic disorder. Up to 50-80% of individuals have associated congenital heart disease. The scope of cardiac disease in NS is quite variable depending on the gene mutation. The most common forms of cardiac defects include pulmonary stenosis, hypertrophic cardiom...