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Cor triatriatum

Cor triatriatum Classification and external resources
ICD-10	Q 24.2
ICD-9	746.82
DiseasesDB	31741
eMedicine	ped/2507 med/458
MeSH	D003310

Cor triatriatum is a congenital heart defect where the left atrium is subdivided.

It can be treated surgically by removing the membrane dividing the atrium.

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This cardiovascular system article is a stub. You can help Wikipedia by expanding it.

v • d • e

Congenital malformations and deformations of circulatory system (Q20-Q28, 745-747)

Cardiac chambers and connections

Persistent truncus arteriosus - Double outlet right ventricle (Taussig-Bing syndrome) - Transposition of the great vessels (dextro, levo)

Ventricular septal defect - Atrial septal defect (Lutembacher's syndrome) - Atrioventricular septal defect (Ostium primum) - Tetralogy of Fallot - Eisenmenger's syndrome

Valvular heart disease/
heart chambers

Right: pulmonary and tricuspid valves	pulmonary valves (stenosis, insufficiency) - tricuspid valves (stenosis, atresia) - Ebstein's anomaly

Left: aortic and mitral valves	aortic valves (stenosis, insufficiency, bicuspid) - mitral valves (stenosis, regurgitation) - Hypoplastic left heart syndrome

Other congenital malformations
of heart

Dextrocardia - Levocardia - Cor triatriatum

aorta (Patent ductus arteriosus, Aortic coarctation, Interrupted aortic arch, Overriding aorta, Aneurysm of sinus of Valsalva, Vascular ring) - Pulmonary atresia

Persistent left superior vena cava - Total anomalous pulmonary venous connection - Scimitar syndrome

Other

Arteriovenous malformation (Cerebral arteriovenous malformation)

See also non-congenital conditions (I, 390-459)

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