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Hypoplastic left heart syndrome (HLHS) is a rare congenital heart defect in which the left side of the heart is severely underdeveloped and incapable of supporting the systemic circulation. [2] It is estimated to account for 2-3% of all congenital heart disease. [ 3 ]
Hypoplastic left heart syndrome, or HLHS, is a congenital heart defect that affects the left side of the heart, specifically affecting the left ventricle and ascending aorta. Also, the aortic valve and mitral valve might be either too small to allow enough blood to flow through, or they might be absent altogether, called atresia.
A number of genetic conditions are associated with heart defects, including Down syndrome, Turner syndrome, and Marfan syndrome. [3] Congenital heart defects are divided into two main groups: cyanotic heart defects and non-cyanotic heart defects , depending on whether the child has the potential to turn bluish in color. [ 3 ]
Trent has hypoplastic left heart syndrome, or HLHS, a rare congenital birth defect that affects normal blood flow through the heart. “Basically, he was born with half a heart,” Holly Williams ...
Hypoplastic left heart syndrome (HLHS) is a rare congenital defect in which a part of the infant's heart is underdeveloped, making it difficult for the left side of the heart to pump enough blood ...
The Fontan Kreutzer procedure is used in pediatric patients who possess only a single functional ventricle, either due to lack of a heart valve (e.g. tricuspid or mitral atresia), an abnormality of the pumping ability of the heart (e.g. hypoplastic left heart syndrome or hypoplastic right heart syndrome), or a complex congenital heart disease where a bi-ventricular repair is impossible or ...
Norwood procedure is most commonly performed to treat hypoplastic left heart syndrome, double outlet right ventricle, double inlet left ventricle, and other single ventricle congenital heart defects. [5] Variations are also used for palliation of mitral and tricuspid atresia [6] and subsets of transposition of great arteries (TGA). [7]
Holt–Oram syndrome: ASD, and a first degree heart block. Hypoplastic left heart syndrome: Jacobsen syndrome: genetic (Chromosome 11q deletion) Jaffe–Campanacci syndrome: Jervell and Lange-Nielsen syndrome: genetic (autosomal recessive) a type of long QT syndrome: Kabuki syndrome: Kearns–Sayre syndrome: Long QT syndrome: Lutembacher's syndrome
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