迈耶-罗基坦斯基-库斯特-豪泽综合征中的慢性肾脏病

Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome.

作者信息

Wani M M, Mir S A

机构信息

Department of Medicine, Al-Amiri Hospital and Al Nafisi dialysis centre, Kuwait.

出版信息

Indian J Nephrol. 2010 Oct;20(4):214-6. doi: 10.4103/0971-4065.73447.

DOI:10.4103/0971-4065.73447

PMID:21206686

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3008953/

Abstract

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by either absence or abnormalities of the mullerian structures. It is a rare disorder, resulting in complete or partial agenesis of the uterus and cervix and primary amenorrhea. It may rarely be associated with anomalies of the urinary tract, ovaries and skeleton. Renal failure secondary to chronic tubulo-interstitial disease has been reported. We report a case of MRKH syndrome presenting late with chronic kidney disease.

摘要

迈耶-罗基坦斯基-库斯特-豪泽（MRKH）综合征的特征是苗勒管结构缺失或异常。它是一种罕见的疾病，导致子宫和宫颈完全或部分发育不全以及原发性闭经。它很少与泌尿道、卵巢和骨骼异常相关。已有继发于慢性肾小管间质性疾病的肾衰竭的报道。我们报告一例出现慢性肾病的晚发性MRKH综合征病例。