BPES is an autosomal dominant, sex-limited condition with a distinctive eyelid phenotype Two forms have been described: in type I, POF related infertility is an adjunct to the condition, and type II is not associated with POF (55). BPES type I is mapped to 3q22-23(54). Two genes are identified within the breakpoint region. One of… Continue reading BPES is an autosomal dominant, sex-limited condition with a distinctive eyelid phenotype