Coexistence of Mayer-Rokitansky-Kuster-Hauser Syndrome and Turner Syndrome: A Case Report

被引：6

作者：

Biaka, Agnieszka ^{[1
]}

Gawlik, Aneta ^{[2
]}

Drosdzol-Cop, Agnieszka ^{[1
]}

Krzysztof, Wilk ^{[1
]}

Maecka-Tendera, Ewa ^{[2
]}

Skrzypulec-Plinta, Violetta ^{[1
]}

机构：

[1] Med Univ Silesia, Sch Hlth Sci Katowice, Katowice, Poland

[2] Med Univ Silesia, Sch Med Katowice, Dept Pediat & Pediat Endocrinol, Katowice, Poland

来源：

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY | 2016年 / 29卷 / 02期

关键词：

Mayer-Rokitansky-Kuster-Hauser syndrome; Turner syndrome; Gonadal dysgenesis;

D O I：

10.1016/j.jpag.2015.10.019

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

Background: Turner syndrome is a common chromosomal disorder, with an incidence of 1 in 2000 live-born female infants. Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) affects 1 in 4500 female births and, rarely, it might be associated with gonadal dysgenesis. Case: A 17-year-old girl was referred to our clinic with short stature and primary amenorrhea. The patient was diagnosed with Turner syndrome and underwent estrogen therapy. At the age of 24 years, just after the patient's sexual initiation, the first complete gynecological examination was performed. A blind-ending vagina was revealed and the patient was diagnosed with MRKH. Summary and Conclusion: Early diagnosis of coexistence of MRKH and Turner syndrome, although very difficult, might prevent patients from developing serious complications.

引用

页码：E35 / E38

页数：4

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