TP63 and 22q11.2 deletion syndrome: The other genetic diagnoses included trisomy 21 (n = 1), trisomy 14 (n = 1), one TP63-mutation associated with ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome 3 (EEC3), sex chromosome anomalies such as Turner (n = 1), and Klinefelter syndromes (n = 1), microdeletions such as 22q11 in DiGeorge syndrome (n = 1).