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 …

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 …

Infertility is considered a major public health issue, and approximately 1 out of 6 people
worldwide suffer from infertility during their reproductive lifespans. Thanks to technological …

Background Approximately 7% of girls will have an anatomic abnormality in their
reproductive tract, diagnosed before or after puberty. Objective It is important for providers to …

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 …

Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome is characterized by Müllerian duct
aplasia in an XX individual with female phenotype presenting primary amenorrhea at …

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

The adrenal cortex undergoes multiple structural and functional rearrangements to satisfy
the systemic needs for steroids during fetal life, postnatal development, and adulthood. A …

Mayer‐Rokitansky‐Küster‐Hauser (MRKH) syndrome is a pathological condition
characterized by primary amenorrhea and infertility and by congenital aplasia of the uterus …