苗勒管发育不全

Also known as Mayer-Rokitansky-Kuster-Hauser syndrome, Mullerian duct failure and hyperandrogenism, WNT4 deficiency, Müllerian duct failure and hyperandrogenism, Müllerian aplasia and hyperandrogenism, MULLERIAN APLASIA AND HYPERANDROGENISM

Key facts

Other names: Rokitansky–Küster–Hauser syndrome (RKH or RKHS) Müller–Mayer–Rokitansky–Küster–Hauser syndrome Müllerian aplasia Vaginal agenesis
Specialty: Gynecology
Symptoms: Missing uterus and variable degrees of vaginal hypoplasia
Causes: Infertility
Frequency: 1 in 4,500 females

via Wikipedia infobox

Research

3,237 papers

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update.Orphanet journal of rare diseases · 2020
Diagnosis and treatment of müllerian malformations.Taiwanese journal of obstetrics & gynecology · 2020
Müllerian Anomalies: Presentation, Diagnosis, and Counseling.Obstetrics and gynecology · 2024
[Mayer-Rokitansky-Küster-Hauser syndrome].

Article · 中文

苗勒管发育不全（英語：Müllerian agenesis），又稱MRKH症候群（Mayer-Rokitansky-Küster-Hauser syndrome），取名于、卡尔·冯·罗基坦斯基、和這四位醫學家，是一类由发育过程中变异而出现的先天性畸形，它导致子宫丧失、阴道上部发育不全。在15%原发性病因闭经病症是苗勒管发育不全引发，包括子宫、宫颈和/或阴道缺失。

Abstract from DBpedia / Wikipedia · CC BY-SA