In this study, we identified 8 deleterious biallelic variants in 6 novel genes, FOXL2, MAJIN, KASH5, SYCP2, MEIOB, and HFM1, in 6 unrelated patients with recurrent HMs and MCs, including one from a familial case of 3 affected members. The gene discussed is FOXL2; the disease is Haim-Munk syndrome.