Comparison of markers of ovarian reserve between patients with complete müllerian agenesis and age-matched fertile and infertile controls

Phenotypic and clinical aspects of Mayer-Rokitansky-Küster-Hauser syndrome in a Chinese population: an analysis of 594 patients

“…Single case studies and small cohort investigations indicate that steroid and pituitary hormone levels in individuals with MRKH fall within the normal limits (10,11). However, some studies have revealed that hormone deregulation could exist in some MRKH patients, as hyperprolactinemia, high progesterone levels, dysregulation of antim€ ullerian hormone levels, differences in luteal phase estrogens, and hypergonadotrophic hypogonadism have been observed (11)(12)(13)(14). Our study used the VCUAM classification system to describe the spectrum of congenital malformations in a large cohort of 623 patients with MRKH syndrome.…”