Ventricular septal defect causes: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Ventricular septal defect}} | {{Ventricular septal defect}} | ||
{{CMG}}, Leida Perez, M.D. | {{CMG}}, Leida Perez, M.D. '''Associate Editor(s)-In-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu], Atif Mohammad, M.D., [[Priyamvada Singh]], [[MBBS]] | ||
'''Associate Editor-In-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu],Atif Mohammad, M.D., [[Priyamvada Singh]], [[MBBS]] | |||
==Overview== | ==Overview== | ||
The causes of [[VSD]] are not fully known. The septal defect between the [[Right ventricle|right]] and [[left ventricle]] can be [[congenital]] that occurs alone or with other [[congenital]] abnormalities. Genetic association suggests the involvement of [[chromosome]] band 22q11 microdeletion in the mechanism of VSD development. In adults, Heart attacks can be complicated by the development of VSD. | |||
==Causes== | ==Causes== | ||
* The causes of VSD are not yet known. This defect often occurs along with other [[congenital heart defects]]. | * The causes of [[VSD]] are not yet known. This defect often occurs along with other [[congenital heart defects]]<ref name="pmid255232322">{{cite journal| author=Spicer DE, Hsu HH, Co-Vu J, Anderson RH, Fricker FJ| title=Ventricular septal defect. | journal=Orphanet J Rare Dis | year= 2014 | volume= 9 | issue= | pages= 144 | pmid=25523232 | doi=10.1186/s13023-014-0144-2 | pmc=4316658 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25523232 }}</ref> | ||
* In adults, ventricular septal | * In adults, [[ventricular septal defect]]<nowiki/>s are a rare but serious [[complication]] of [[heart attacks]]. These holes are related to [[heart attacks]] and do not result from a birth defect. | ||
* Genetics - The frequent association between arch abnormalities and significant conal VSDs suggests a common mechanism involving a chromosome band 22q11 microdeletion. Deletions in this area have not been linked with isolated supracristal VSDs. | *[[Genetics]] - The frequent association between arch abnormalities and significant conal [[VSD|VSDs]] suggests a common mechanism involving a [[chromosome]] band 22q11 microdeletion. Deletions in this area have not been linked with isolated supracristal [[VSD|VSDs]]. | ||
* Maternal Drug use - [[Clomifene]] | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Cardiology]] | |||
[[Category:Congenital heart disease]] | |||
[[Category:Pediatrics]] | |||
[[Category:Disease]] | |||
[[Category:Needs overview]] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Latest revision as of 21:10, 18 February 2020
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Ventricular septal defect Microchapters | |
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Differentiating Ventricular Septal Defect from other Diseases | |
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Diagnosis | |
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ACC/AHA Guidelines for Surgical and Catheter Intervention Follow-Up | |
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Case Studies | |
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Ventricular septal defect causes On the Web | |
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American Roentgen Ray Society Images of Ventricular septal defect causes | |
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Risk calculators and risk factors for Ventricular septal defect causes | |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1], Leida Perez, M.D. Associate Editor(s)-In-Chief: Keri Shafer, M.D. [2], Atif Mohammad, M.D., Priyamvada Singh, MBBS
Overview
The causes of VSD are not fully known. The septal defect between the right and left ventricle can be congenital that occurs alone or with other congenital abnormalities. Genetic association suggests the involvement of chromosome band 22q11 microdeletion in the mechanism of VSD development. In adults, Heart attacks can be complicated by the development of VSD.
Causes
- The causes of VSD are not yet known. This defect often occurs along with other congenital heart defects[1]
- In adults, ventricular septal defects are a rare but serious complication of heart attacks. These holes are related to heart attacks and do not result from a birth defect.
- Genetics - The frequent association between arch abnormalities and significant conal VSDs suggests a common mechanism involving a chromosome band 22q11 microdeletion. Deletions in this area have not been linked with isolated supracristal VSDs.
- Maternal Drug use - Clomifene
References
- ↑ Spicer DE, Hsu HH, Co-Vu J, Anderson RH, Fricker FJ (2014). "Ventricular septal defect". Orphanet J Rare Dis. 9: 144. doi:10.1186/s13023-014-0144-2. PMC 4316658. PMID 25523232.