AMHR2 and Azoospermia: Compound heterozygous mutations in c.494_502del (p.I165_A168delinsT) in exon 4 and g.6147C>A of AMHR2 (NM_001164690 transcript) were identified in case 2, who had a history of left laparoscopic hernia repair and bilateral laparoscopic orchiopexy as well as infertility due to azoospermia.