Aortic arch anomalies causes: Difference between revisions

	Aortic arch anomalies Microchapters
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Latest revision as of 21:54, 14 March 2016

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 {{Aortic arch anomalies}}
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-{{CMG}}
-'''Associate Editor-In-Chief:''' {{CZ}} [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu] [[Priyamvada Singh|Priyamvada Singh, MBBS]] [[mailto:psingh@perfuse.org]]
-'''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [[mailto:kfeeney@perfuse.org]]
-==Causes==
-===Genetics===
-====Double Aortic Arch====
-Double aortic arch is associated with a chromosome band 22q11 deletion in approximately 20% of patients. Double aortic arch may be associated with band 22q11 deletion, which has various other possible manifestations. These include, but are not limited to, palatal abnormalities, laryngotracheal anomalies, speech and learning delay, characteristic facial features, [[hypocalcemia]], abnormalities of T-cell–mediated immune function, and neurologic defects.
 ==References==
-{{reflist}}
+{{reflist|2}}
-==External Links==
+{{WH}}
-* [http://www.ajronline.org/cgi/reprint/116/1/125 Double Aortic Arch]
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+[[CME Category::Cardiology]]
-== Acknowledgements ==
-The content on this page was first contributed by: C. Michael Gibson, M.S., M.D.
 [[Category:Cardiovascular system]]
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 [[Category:Pediatrics]]
 [[Category:Pulmonology]]
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