Autosomal dominant forms include DKCA2 (OMIM#613989), DKCA3 (OMIM#613990), DKCA4 (OMIM#615190), DKCA5 (Revesz Syndrome, OMIM#268130), and DKCA6 (OMIM#616553). The gene discussed is TINF2; the disease is Revesz syndrome.