Patterns of cardiac and extracardiac anomalies in adults with tetralogy of Fallot

BACKGROUND: Tetralogy of Fallot (TOF) is a complex congenital heart disease with clinical and genetic heterogeneity. Of the few known causes, 22q11.2 deletion syndrome (22q11DS) is the most common. We sought to define other clinical subgroups by focusing on cardiac and extracardiac features. METHODS...

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Bibliografiset tiedot
Päätekijät: Piran, Sara, Bassett, Anne S., Grewal, Jasmine, Swaby, Jodi-Ann, Morel, Chantal, Oechslin, Erwin N., Redington, Andrew N., Liu, Peter P., Silversides, Candice K.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3142274/
https://ncbi.nlm.nih.gov/pubmed/21167345
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ahj.2010.09.015
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