Conotruncal anomaly face syndrome

DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental delay, learning problems and cleft palate. [Source: Wikipedia ]

May Cause
Congenital heart disease
May Be Caused by
Chromosome 22q11.2 deletion