WFS1 and Wolfram syndrome: Within our cohort, three identified genes—TECTA (ATS3A and ATS3B), COL4A3 (DFNA8/12 and DFNB21), and WFS1 (DFNA6/14/38 and Wolfram syndrome)—are known to have exhibited both autosomal recessive and autosomal dominant inheritance patterns (https://hereditaryhearingloss.org/).