Abnormalities seen in the four-chamber view
Tricuspid Valve Dysplasia
In this condition, the position of the tricuspid valve is normal but the leaflets are dysplastic. The tricuspid valve is incompetent, demonstrated by colour Doppler showing tricuspid regurgitation, and the right atrium is dilated. Significant cardiomegaly may cause secondary lung compression and consequent hypoplasia. Severe cases can result in fetal hydrops and subsequent death. In severe cases of tricuspid valve dysplasia there is pulmonary stenosis or functional atresia.
Prevalence
This defect is found in less than 1 in 20,000 live births.
Other abnormalities
This defect is commonly associated with chromosomal anomalies, mainly Trisomy 18.
Prognosis
If cardiac anomaly is isolated, prognosis is guarded in those cases where there is a severe tricuspid valve regurgitation and cardiomegaly.
A case of tricuspid valve dysplasia
There is severe cardiomegaly mainly due to significantly enlarged right atrium. There are normal atrioventricular connections. The tricuspid valve appears dysplastic and the colour Doppler indicates significant regurgitation (white arrowhead). Note that in contrast to Ebstein’s anomaly, there is normal offsetting of the atrioventricular valves.