FBN1 and androgen insensitivity syndrome: Bibliometric analysis based on the reports about AIS risk found that high frequent polymorphism in fibrillin (FBN) gene, estrogen receptor gene, calmodulin, collagen gene and Ladybird Homeobox 1 (LBX1) might involve in physiological or (and) pathological processes, such as menarche, Bone formation, disc degeneration, melatonin signaling dysfunction, and cerebrospinal fluid flow in AIS (Jiang S. et al., 2023).