Double orifice mitral valve (DOMV) is a rare congenital heart anomaly characterized by the presence of two distinct orifices in the mitral valve instead of the usual single orifice. This comprehensive article aims to provide a thorough understanding of double orifice mitral valve, including its anatomy, symptoms, diagnosis, and treatment options.
In individuals with double orifice mitral valve, the valve leaflets are divided into two separate orifices by a central fibrous bridge or a "double flap" arrangement. This results in the formation of two distinct pathways for blood flow through the mitral valve.
The symptoms of double orifice mitral valve can vary depending on the severity of the anomaly and associated complications. Common symptoms may include:
The diagnosis of double orifice mitral valve typically involves a combination of imaging studies and clinical evaluation. Diagnostic methods may include:
The management of double orifice mitral valve depends on the severity of symptoms, the degree of valve dysfunction, and associated complications. Treatment options may include:
The prognosis for individuals with double orifice mitral valve depends on the severity of the anomaly, associated cardiac abnormalities, and the effectiveness of treatment. With appropriate management and follow-up care, most individuals can lead normal lives. Regular follow-up visits with a cardiologist are important to monitor the individual's condition, assess valve function, and address any potential complications.
Double orifice mitral valve is a rare congenital heart anomaly characterized by the presence of two distinct orifices in the mitral valve. By understanding its anatomy, symptoms, diagnosis, and treatment options, healthcare professionals can provide appropriate management and improve outcomes for individuals with double orifice mitral valve.
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