Cyanosis screening: Difference between revisions
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==Overview== | ==Overview== | ||
==Screening== | ==Screening== | ||
Prenatal [[echocardiography]] and genetic testing are useful methods for early detection of [[cyanotic]] [[congenital heart disease]]. | *Prenatal [[echocardiography]] and genetic testing are useful methods for early detection of [[cyanotic]] [[congenital heart disease]]. | ||
*Postnatal [[pulse oximetry]] is recommended for diagnosis of [[cyanotic]] [[congenital heart disease]]. | |||
==References== | ==References== | ||
Revision as of 17:10, 6 November 2020
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Cyanosis Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Cyanosis screening On the Web |
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American Roentgen Ray Society Images of Cyanosis screening |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Screening
- Prenatal echocardiography and genetic testing are useful methods for early detection of cyanotic congenital heart disease.
- Postnatal pulse oximetry is recommended for diagnosis of cyanotic congenital heart disease.