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    VENTRICULAR SEPTAL DEFECTS

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    azu_etd_hr_2023_0121_sip1_m.pdf
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    Author
    Liong, Maria
    Issue Date
    2023
    Advisor
    Cohen, Zoe
    
    Metadata
    Show full item record
    Publisher
    The University of Arizona.
    Rights
    Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
    Abstract
    Ventricular septal defects (VSD) are one of the most common congenital defects in children. They differ in size and have four differen t types consisting of membranous, trabecular, inlet, and supracristal based on where exactly on the ventricular septum they are found. There are a wide variety of tests that can diagnose and confirm VSD such as echocardiograms, electrocardiograms, X rays, computed tomography scans, and cardiac catheterization. Genetic risk factors have not yet bee n pinpointed, although other risk factors for VSDs are similar to those of other congenital defects. VSDs are often present in Trisomy 21 cases and can cause serious com plications if they go untreated. One of the most serious of those complications is Eisenmenger syndrome, which cannot be corrected with surgery. While medications can aid with symptoms of VSDs, they cannot cure the defects themselves and thus treatment opt ions include: waiting for the defect to close on its own, surgical closure of the defect, or correction using transcatheter devices. New research understanding both why VSDs occur and new methods with which they can be corrected can help lower these risks both short term and long term for our children of the future.
    Type
    Electronic thesis
    text
    Degree Name
    B.S.
    Degree Level
    bachelors
    Degree Program
    Physiology and Medical Sciences
    Honors College
    Degree Grantor
    University of Arizona
    Collections
    Honors Theses

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