Abstract Background Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, also referred to
as Müllerian aplasia, is a congenital disorder characterized by aplasia of the uterus and …

Androgen insensitivity syndrome in its complete form is a disorder of hormone resistance
characterised by a female phenotype in an individual with an XY karyotype and testes …

Background Despite evidence that genetic factors contribute to the duration of gestation and
the risk of preterm birth, robust associations with genetic variants have not been identified …

Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome, also referred to as Müllerian
agenesis, is the second most common cause of primary amenorrhea. It is characterized by …

The reproductive endocrine systems are vastly different between males and females. This
sexual dimorphism of the endocrine milieu originates from sex-specific differentiation of the …

Zusammenfassung Das Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrom [MIM 277000]
ist durch einen fehlenden Uterus und eine fehlende Vagina bei phänotypisch unauffälligen …

The Müllerian ducts are part of the embryonic urogenital system. They give rise to mature
structures that serve a critical function in the transport and development of the oocyte and/or …

There is emerging evidence that early uterine development in humans is an important
determinant of conditions such as ontogenetic progesterone resistance, menstrual …

The two main functions of the ovary are the production of oocytes, which allows the
continuation of the species, and secretion of female sex hormones, which control many …

Disorders (or differences) of sex development (DSD) are a heterogeneous group of
congenital conditions with variations in chromosomal, gonadal, or anatomical sex. Impaired …