Taussig-Bing syndrome

Taussig-Bing syndrome

Infobox_Disease
Name = PAGENAME


Caption =
DiseasesDB = 32215
ICD10 = ICD10|Q|20|1|q|20
ICD9 = ICD9|745.11
ICDO =
OMIM = 217095
MedlinePlus =
eMedicineSubj = ped
eMedicineTopic = 2509
eMedicine_mult = eMedicine2|ped|2508 | MeshID = D004310

Taussig-Bing syndrome is a cyanotic congenital heart defect (CHD) in which the patient has both double outlet right ventricle (DORV) and subpulmonic ventricular septal defect (VSD).

In DORV, instead of the normal situation where blood from the left ventricle (LV) flows out to the aorta and blood from the right ventricle (RV) flows out to the pulmonary artery, both aorta and pulmonary artery are connected to the RV, and the only path for blood from the LV is across the VSD. When the VSD is subpulmonic (sitting just below the pulmonary artery), the LV blood then flows preferentially to the pulmonary artery. Then the RV blood, by default, flows mainly to the aorta.

The clinical manifestations of a Taussig-Bing anomaly, therefore, are much like those of dextro-Transposition of the great arteries (but the surgical repair is different).


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