苗勒管发育不全 - 维基百科，自由的百科全书
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 奥格斯特·佛列斯·杰斯佛·卡尔·苗勒 、 卡尔·冯·罗基坦斯基 、 赫尔曼·卡斯特 和 G.A.豪泽 這四位醫學家，是一类由 苗勒管 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 [1]。 苗勒管发育不全的患者激素正常，这意味着他们将有 第二性 …
Mayer-Rokitansky-Küster-Hauser Syndrome - Cleveland Clinic
Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is a rare congenital disorder that can affect women and people assigned female at birth (AFAB). It’s a condition that causes your vagina and uterus to be missing or underformed. In most cases, your ovaries and fallopian tubes function normally, and your external genitals are unaffected.
Mayer-Rokitansky-Küster-Hauser syndrome - MedlinePlus
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a disorder that mainly affects the female reproductive system. This condition causes the vagina and uterus to be underdeveloped or absent, although external genitalia are normal. Affected individuals usually do not have menstrual periods due to the absence of a uterus.
Müllerian agenesis - Wikipedia
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.
什么是MRKH？ - 知乎专栏
2023年4月27日 · MRKH综合征是一种先天性女性生殖系统畸形，发生率约为1/5000～1/4000，表现为先天性无阴道和 (或)阴道发育不良、无子宫或始基子宫，卵巢功能多为正常。 那么什么是MRKH？ 1.月经初潮时间晚：月经初潮一般为13-15岁，…
Mayer-Rokitansky-Küster-Hauser Syndrome - Symptoms, Causes, …
2014年7月4日 · Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare disorder that affects women. It is characterized by the failure of the uterus and the vagina to develop properly in women who have normal ovarian function and normal external genitalia.
先天性无阴道综合征的影像学解析 - 丁香园 - DXY.cn
2015年7月10日 · 先天性无阴道综合征（Mayer-Rokitansky-Küster-Hauser syndrome， MRKH 综合征）为女性胚胎期发育受到内在或外界因素阻扰，引起副中肾管发育异常所致的一系列临床体征，在中国古代，将患有该病的女子称为「石女」，根据资料报道，其发生率约为 1/4000-1/5000。 患者在幼年时多为无症状，大多是在青春期因原发性闭经而就诊时被发现。 其临床表现根据分型多有不同，下面是一例由 Mahyar 博士提供的 MRKH 综合征的典型案例，我们一起通过影像学 …
Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome - Penn …
Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome is a rare congenital disorder that affects the female reproductive system. This condition is characterized by an underdeveloped vagina and uterus. The uterus may be small or absent and the vagina is typically shortened. People with MRKH have normally-functioning ovaries and a female chromosome pattern.
Mayer-Rokitansky-Küster-Hauser syndrome - Radiopaedia.org
2024年12月21日 · Mayer-Rokitansky-Küster-Hauser syndrome (MRKH), also known as Müllerian aplasia, is a congenital anomaly characterized by vaginal and uterine aplasia or agenesis 9. It is usually also associated with a spectrum of other genitourinary tract abnormalities. MRKH syndrome belongs to class I Mullerian duct anomalies. Two different forms are described:
Mayer-Rokitansky-Kuster-Hauser Syndrome: Embryology, Genetics …
2022年2月13日 · Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a pathological condition characterized by primary amenorrhea and infertility and by congenital aplasia of the uterus and of the upper vagina. The development of secondary sexual characters is normal as well as that the karyotype (46,XX).