Open access
Aug 2026
Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism
This is the first report of concurrent CAIS and NF1, which enriches and expands the genotypic and phenotypic spectra of both disorders.
Wei Wang, Yake Jiao, Yang Xiu et al.
· Frontiers in Pediatrics · 0 citations