Taussig–Bing syndrome: Difference between revisions
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{{Infobox_Disease | |
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Name = {{PAGENAME}} | |
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Image = | |
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Caption = | |
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DiseasesDB = 32215 | |
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ICD10 = Q20.2 | |
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ICD9 = | |
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ICDO = | |
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OMIM = 217095 | |
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MedlinePlus = | |
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eMedicineSubj = ped | |
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eMedicineTopic = 2509 | |
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eMedicine_mult = {{eMedicine2|ped|2508}} | |
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'''Taussig-Bing syndrome''' is a [[cyanotic heart defect|cyanotic]] [[congenital]] [[congenital heart defect|heart defect]] ('''CHD''') in which the patient has both [[double outlet right ventricle]] ('''DORV''') and [[anatomical_position#Coronal_plane|anterior]] [[ventricular septal defect]] ('''VSD'''). |
'''Taussig-Bing syndrome''' is a [[cyanotic heart defect|cyanotic]] [[congenital]] [[congenital heart defect|heart defect]] ('''CHD''') in which the patient has both [[double outlet right ventricle]] ('''DORV''') and [[anatomical_position#Coronal_plane|anterior]] [[ventricular septal defect]] ('''VSD'''). |
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Revision as of 14:23, 2 September 2006
| Taussig–Bing syndrome | |
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| Specialty | Medical genetics  |
Taussig-Bing syndrome is a cyanotic congenital heart defect (CHD) in which the patient has both double outlet right ventricle (DORV) and anterior ventricular septal defect (VSD).
 | This cardiovascular system article is a stub. You can help Wikipedia by expanding it. |