Search results
Results from the WOW.Com Content Network
Congenital heart defect. A congenital heart defect (CHD), also known as a congenital heart anomaly, congenital cardiovascular malformation, and congenital heart disease, is a defect in the structure of the heart or great vessels that is present at birth. [ 7 ] A congenital heart defect is classed as a cardiovascular disease. [ 10 ]
The Children's Heart Foundation is hosting one of its 33 heart walks in Gilbert to raise awareness for what the CDC says is the most common type of defects in newborns.
CDK13-related disorder, also known as congenital heart defects, dysmorphic facial features and intellectual developmental disorder (CHDFIDD), is a very rare autosomal dominant genetic condition characterised by congenital heart defects, intellectual disability and characteristic facial features. Those affected typically have motor and language ...
Eisenmenger syndrome or Eisenmenger's syndrome is defined as the process in which a long-standing left-to-right cardiac shunt caused by a congenital heart defect (typically by a ventricular septal defect, atrial septal defect, or less commonly, patent ductus arteriosus) causes pulmonary hypertension [1] [2] and eventual reversal of the shunt into a cyanotic right-to-left shunt.
The diagnosis of a congenital heart defect in a newborn or unborn child is unquestionably alarming news for parents and parents-to-be. They may wonder if their child is going to be okay, and what ...
A Washington State University sophomore on the school's cheer team, Reyes, 19, knows what it's like to have heart issues as a survivor of a congenital heart defect called Tetralogy of Fallot.
Cardiology. Ebstein's anomaly is a congenital heart defect in which the septal and posterior leaflets of the tricuspid valve are displaced downwards towards the apex of the right ventricle of the heart. [1] EA has great anatomical heterogeneity that generates a wide spectrum of clinical features at presentation and is complicated by the fact ...
DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. [7] While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental disability, intellectual disability and cleft palate. [7]