Antenatal detection and diagnosis: Difference between revisions

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New page: {{Congenital heart disease}} {{CMG}} '''Associate Editor-In-Chief:''' Keri Shafer, M.D. [mailto:kshafer@bidmc.harvard.edu] '''Associate Editor-In-Chief:''':Atif Moh...
 
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{{Congenital heart disease}}
{Congenital heart disease}}


{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh@perfuse.org],[[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu], Atif Mohammad, M.D.; '''Assistant Editor(s)-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@perfuse.org]


{{CMG}}
==Overview===
 
'''Associate Editor-In-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu]
 
'''Associate Editor-In-Chief:''':Atif Mohammad, M.D.
 
__NOTOC__
 
[[Antenatal Detection and Diagnosis]]
[[Antenatal Detection and Diagnosis]]
Before birth, an obstetric ultrasound scan may be used to screen pregnant women for signs of CHD in their unborn babies. This screening scan is often performed around 20 weeks of pregnancy when the fast moving structures of the fetal heart are large enough to be more easily imaged.   
Before birth, an obstetric ultrasound scan may be used to screen pregnant women for signs of CHD in their unborn babies. This screening scan is often performed around 20 weeks of pregnancy when the fast moving structures of the fetal heart are large enough to be more easily imaged.   
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It is increasingly possible for specialists to screen for CHD as early as 14 weeks, if CHD is suspected from other factors, such as a family history.
It is increasingly possible for specialists to screen for CHD as early as 14 weeks, if CHD is suspected from other factors, such as a family history.


==References==
{{Reflist|2}}
{{Reflist|2}}
{{Congenital malformations and deformations of circulatory system}}
{{SIB}}


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[[Category:Cardiology]]
[[Category:Cardiology]]
[[Category:Congenital heart disease]]
[[Category:Congenital heart disease]]
[[Category:Genetic Disease]]
[[Category:Genetic disease]]
[[Category:Pediatrics]]


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Revision as of 16:13, 15 August 2011

{Congenital heart disease}}

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2],Keri Shafer, M.D. [3], Atif Mohammad, M.D.; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S. [4]

Overview=

Antenatal Detection and Diagnosis Before birth, an obstetric ultrasound scan may be used to screen pregnant women for signs of CHD in their unborn babies. This screening scan is often performed around 20 weeks of pregnancy when the fast moving structures of the fetal heart are large enough to be more easily imaged. If CHD is suspected, a mother will be referred for a fetal echocardiograph, which is a more detailed, diagnostic ultrasound scan by a specialist cardiologist. It is increasingly possible for specialists to screen for CHD as early as 14 weeks, if CHD is suspected from other factors, such as a family history.

References

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