To date, there are no diagnostic criteria for CFC syndrome, so a suspected diagnosis is usually made based on conspicuous clinical findings and confirmed by genetic diagnostics.<\/p>\n<\/div>
Suspected Diagnosis<\/h4><\/div><\/div><\/div>
CFC syndrome is suspected if the following findings are present:<\/p>\n<\/div>
Heart:<\/h4><\/div>\n- Pulmonary stenosis (narrowing of the outflow tract from the right ventricle to the pulmonary artery)<\/li>\n
- Atrial septal defect (hole in the cardiac septum between the two atria of the heart)<\/li>\n
- Ventricular septal defect (hole in the ventricular septum between the two chambers of the heart)<\/li>\n
- Hypertrophic cardiomyopathy (thickening of the heart muscles, usually of the left ventricle)<\/li>\n
- Heart valve defects<\/li>\n
- Rhythm disturbances<\/li>\n<\/ul>\n<\/div>
Head and Face:<\/h4><\/div>