Ten molar tissues from the patients with P/LP biallelic variants in FOXL2 (n = 4), MAJIN (n = 2), SYCP2 (n = 1), HFM1 (n = 1), and MEIOB (n = 1) were available for morphological reevaluation and four for immunohistochemistry with p57, and their diagnosis was confirmed as CHM. This evidence concerns the gene FOXL2 and choroideremia.