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Learn about the causes, diagnosis, and treatment options for müllerian agenesis, a rare condition that affects the development of the vagina and uterus. This web page provides recommendations and conclusions from the American College of Obstetricians and Gynecologists based on evidence and expert opinion.
Müllerian agenesis, also known as Müllerian aplasia, vaginal agenesis, or Mayer–Rokitansky–Küster–Hauser syndrome (MRKH syndrome), is a congenital malformation characterized by a failure of the Müllerian ducts to develop, resulting in a missing uterus and variable degrees of vaginal hypoplasia of its upper portion.
20 de ago. de 2020 · Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome [ICD-10 Q51.0/Q52.0; OMIM %277000/%601076; ORPHA 3109], also referred to as Müllerian aplasia or congenital absence of the uterus and vagina, is a congenital disorder characterized by agenesis or aplasia of the uterus and upper part of the vagina in females with a normal female ...
9 de feb. de 2024 · MRKH syndrome, also known as Müllerian aplasia, is a congenital anomaly of the uterus and upper vagina. It is associated with other genitourinary tract abnormalities, such as renal anomalies and vertebral defects.
MRKH syndrome, also known as Müllerian agenesis or vaginal agenesis, is a rare condition that affects one in 4,500 people assigned female at birth. It causes underdevelopment of the uterus, cervix and upper vagina, leading to amenorrhea and infertility. Learn about the diagnosis, treatment and prognosis of MRKH syndrome.
Mullerian agenesis, a congenital malformation of the genital tract is the second most common cause of primary amenorrhea. Its etiology is poorly understood but it may be associated with renal, skeletal, and other abnormalities.
1 de oct. de 2021 · Müllerian agenesis, also known as Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), refers to a group of female genital tract anomalies caused by interrupted development of the müllerian ducts, resulting in agenesis or hypoplasia of the uterus and vagina.
