Systemic Hemochromatosis
Young adult with unusual clinical presentation and rare genetic mutation. Diagnosis unfolds with CMR!

Young adult with unusual clinical presentation and rare genetic mutation. Diagnosis unfolds with CMR!
MYH7 is the 3rd commonest inheritable cause of genetic dilated cardiomyopathy. All ”idiopathic” DCMs must have genetic testing done to determine prognosis, arrhythmogenic vs heart failure possibilities and to diagnose possible disease in family members if a definite gene is identified
A snippet on tumors that in most instances can be readily diagnosed.