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Tetralogy of Fallot (TOF)
Tetralogy of Fallot is 4 congenital heart defects. This means that your child is born with them. These 4 problems occur together (tetralogy refers to 4).
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Transposition of the Great Arteries (TGA) in Children
Transposition of the great arteries (TGA) is a type of congenital heart defect. This means that your baby is born with it. In this condition, the large blood vessels that carry blood from the heart to the lungs and body aren’t connected as they should be.
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Truncus Arteriosus (TA)
Truncus arteriosus is a heart defect that is present at birth (congenital). It occurs when there is an abnormal connection between the aorta and pulmonary artery. Normally, the aorta and the pulmonary artery are separate. Read on to learn more.
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Tilt Table Test for Children
The tilt table test is done to find the cause of fainting (syncope). Tilt table testing is done with a special table or bed that changes a child's position from lying to standing. Their blood pressure and heart rate are checked while they're in the different positions.
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Ultrafast CT Scan for Children
An ultrafast computed tomography (CT) scan is an imaging test that uses X-rays and a computer to look at your child’s heart. It gives the doctor many details about your child’s heart that other imaging tests can’t. Learn more about what you can expect when your child has this test.
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Ventricular Septal Defect (VSD) in Children
A ventricular septal defect (VSD) is a congenital heart defect. This means that your baby is born with it. A VSD is an opening or hole in the dividing wall (septum) between the 2 lower chambers of the heart (right and left ventricles). VSDs are the most common type of congenital heart defect.
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Overview of Craniofacial Anomalies
Detailed information on craniofacial anomalies, including cleft lip, cleft palate, craniosynostosis, hemifacial microsomia, vascular malformation, hemangioma, and deformational plagiocephaly.
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The Craniofacial Team
Read this for information about a first assessment of any craniofacial abnormalities your child may have and the craniofacial treatment team that will treat them.
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Hemifacial Microsomia (HFM) in Children
Hemifacial microsomia (HFM) is a congenital disorder. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped (hemi means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.
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Showing 8155 - 8163 of 11277 results