Taussig–Bing syndrome: Difference between revisions
No edit summary |
Bsadowski1 (talk | contribs) m Reverted edit by Rvoutletss (talk) to last version by Ozzie10aaaa |
||
| (4 intermediate revisions by 4 users not shown) | |||
| Line 2: | Line 2: | ||
{{Infobox medical condition (new) |
{{Infobox medical condition (new) |
||
| name = {{PAGENAME}} |
| name = {{PAGENAME}} |
||
| synonyms = |
| synonyms = |
||
| image = |
| image = |
||
| width = |
| width = |
||
| alt = |
| alt = |
||
| caption = |
| caption = |
||
| pronounce = |
| pronounce = |
||
| specialty = [[Cardiac surgery]] |
| specialty = [[Cardiac surgery]] |
||
| symptoms = |
| symptoms = |
||
| Line 13: | Line 13: | ||
| onset = |
| onset = |
||
| duration = |
| duration = |
||
| types = |
| types = |
||
| causes = |
| causes = |
||
| risks = |
| risks = |
||
| diagnosis = |
| diagnosis = |
||
| differential = |
| differential = |
||
| Line 23: | Line 23: | ||
| prognosis = |
| prognosis = |
||
| frequency = |
| frequency = |
||
| deaths = |
| deaths = |
||
}} |
}} |
||
'''Taussig–Bing syndrome''' is a [[cyanotic heart defect|cyanotic]] [[congenital]] [[congenital heart defect|heart defect]]<ref>{{Cite journal|last=Konstantinov|first=Igor E.|date=2009|title=Taussig-Bing Anomaly|journal=Texas Heart Institute Journal|volume=36|issue=6|pages=580–585|issn=0730-2347|pmc=2801930|pmid=20069085}}</ref> in which the patient has both [[double outlet right ventricle]] (DORV) and [[subpulmonic]] [[ventricular septal defect]] (VSD).<ref>{{cite book|last1=Ramrakha|first1=Punit S.|last2=Ramrakha|first2=Punit|last3=Hill|first3=Jonathan|title=Oxford Handbook of Cardiology|date=2012|publisher=OUP Oxford|isbn=9780199643219|page=707|language=en}}</ref> |
'''Taussig–Bing syndrome''' is a [[cyanotic heart defect|cyanotic]] [[congenital]] [[congenital heart defect|heart defect]]<ref>{{Cite journal|last=Konstantinov|first=Igor E.|date=2009|title=Taussig-Bing Anomaly|journal=Texas Heart Institute Journal|volume=36|issue=6|pages=580–585|issn=0730-2347|pmc=2801930|pmid=20069085}}</ref> in which the patient has both [[double outlet right ventricle]] (DORV) and [[subpulmonic]] [[ventricular septal defect]] (VSD).<ref>{{cite book|last1=Ramrakha|first1=Punit S.|last2=Ramrakha|first2=Punit|last3=Hill|first3=Jonathan|title=Oxford Handbook of Cardiology|date=2012|publisher=OUP Oxford|isbn=9780199643219|page=707|language=en}}</ref> |
||
| Line 31: | Line 31: | ||
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). It can be corrected surgically also with the arterial switch operation (ASO). |
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). It can be corrected surgically also with the arterial switch operation (ASO). |
||
It is managed with [[Rastelli procedure]]. It is named after [[Helen B. Taussig]] and [[Richard Bing]]. |
It is managed with [[Rastelli procedure]]. It is named after [[Helen B. Taussig]] and [[Richard Bing]], who first described it in 1949.<ref>{{Cite journal|last=Konstantinov|first=Igor E.|date=2009|title=Taussig-Bing Anomaly|journal=Texas Heart Institute Journal|volume=36|issue=6|pages=580–585|issn=0730-2347|pmc=2801930|pmid=20069085}}</ref> |
||
==References== |
==References== |
||
| Line 46: | Line 46: | ||
| eMedicineSubj = ped | |
| eMedicineSubj = ped | |
||
| eMedicineTopic = 2509 | |
| eMedicineTopic = 2509 | |
||
| eMedicine_mult = {{eMedicine2|ped|2508}} | |
| eMedicine_mult = {{eMedicine2|ped|2508}} | |
||
| MeshID = D004310 | |
| MeshID = D004310 | |
||
}} |
}} |
||
Latest revision as of 10:54, 5 January 2024
 | This article needs additional citations for verification. (May 2018) |
| Taussig–Bing syndrome | |
|---|---|
| Specialty | Cardiac surgery |
Taussig–Bing syndrome is a cyanotic congenital heart defect[1] in which the patient has both double outlet right ventricle (DORV) and subpulmonic ventricular septal defect (VSD).[2]
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). It can be corrected surgically also with the arterial switch operation (ASO).
It is managed with Rastelli procedure. It is named after Helen B. Taussig and Richard Bing, who first described it in 1949.[3]
References
[edit]- ^ Konstantinov, Igor E. (2009). "Taussig-Bing Anomaly". Texas Heart Institute Journal. 36 (6): 580–585. ISSN 0730-2347. PMC 2801930. PMID 20069085.
- ^ Ramrakha, Punit S.; Ramrakha, Punit; Hill, Jonathan (2012). Oxford Handbook of Cardiology. OUP Oxford. p. 707. ISBN 9780199643219.
- ^ Konstantinov, Igor E. (2009). "Taussig-Bing Anomaly". Texas Heart Institute Journal. 36 (6): 580–585. ISSN 0730-2347. PMC 2801930. PMID 20069085.
External links
[edit]