 Chris Crossheart, CCH, is a rare congenital cardiac malformation characterized by the presence of two separate ventricular septums which cross each other at the level of the mitral valves. It is often associated with cyanotic heart disease, coarctation of the aorta, and mitral valve lesions. Echocardiography is the gold standard for diagnosing this condition, as it allows for accurate visualization of the heart structure and function. Early detection and treatment are essential for improving patient outcomes and increasing survival rates. This paper presents a case series of patients diagnosed with CCH, highlighting the importance of early diagnosis and intervention. This article was authored by Abdul Malik Sheikh, Asma Kinval, and Hina Sattar.