ADAMTS17 and Weill-Marchesani 4 syndrome, recessive: Biallelic disease-causing variants in ADAMTSL2 (geleophysic dysplasia type 1, n = 4), ADAMTS10 (Weill-Marchesani syndrome type 1 (WMS1), n = 3), and ADAMTS17 (Weill-Marchesani syndrome type 4 (WMS4), n = 1) were identified.