Long-term follow-up on MURCS (müllerian duct, renal, cervical somite dysplasia) association and a review of the literature

Citations

SCOPUS

3

초록

Müllerian duct aplasia-renal aplasia-cervicothoracic somite dysplasia (MURCS) association is a unique development disorder with four common types of malformations that include uterine aplasia or hypoplasia, renal ectopy or agenesis, vertebral anomalies, and short stature. The majority of MURCS patients are diagnosed with primary amenorrhea from late-adolescence. However, a few cases with MURCS association are not well diagnosed during childhood and long-term outcomes are not well reported. We report a case of an 8-year-old girl with MURCS association who presented with recurrent urinary tract infections and multiple congenital malformations, and who was followed for 10 years until adulthood. MURCS association should be considered as one of the differential diagnoses when evaluating prepubertal females with vertebral and renal malformations. © 2019 Annals of Pediatric Endocrinology & Metabolism.

키워드

ChildMayer-rokitansky-küster-hauser anomalyMullerian aplasiaMüllerian duct aplasia-renal aplasia-cervicothoracic somite dysplasia association
제목
Long-term follow-up on MURCS (müllerian duct, renal, cervical somite dysplasia) association and a review of the literature
저자
Kim, SunLee, Yeong SeokKim, Dong HyunYang, AramLee, TackHwang, Seun DeukKwon, Dae GyuLee, Ji Eun
DOI
10.6065/apem.2019.24.3.207
발행일
2019
유형
Article
저널명
Annals of Pediatirc Endocrinology & Metabolism
24
3
페이지
207 ~ 211