A Chorionic Gonadotropin–Sensitive Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Gestational Spontaneous Ovarian Hyperstimulation Syndrome

Abstract

This Brief Report describes recurrent gestational spontaneous ovarian hyperstimulation syndrome in a family with a heterozygous mutation in the transmembrane domain of the receptor for follicle-sti...