Antenatal detection and diagnosis: Difference between revisions
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... |
No edit summary |
||
Line 1: | Line 1: | ||
{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] | |||
==Overview=== | |||
[[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. | ||
Line 15: | Line 9: | ||
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}} | ||
[[de:Herzfehler]] | [[de:Herzfehler]] | ||
Line 35: | Line 26: | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Congenital heart disease]] | [[Category:Congenital heart disease]] | ||
[[Category:Genetic | [[Category:Genetic disease]] | ||
[[Category:Pediatrics]] | |||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} |
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
de:Herzfehler lv:Iedzimtās sirds slimības nn:Medfødd hjartefeil sr:Урођене срчане мане uk:Вроджені вади серця wa:Maladeye des bleus påpåds