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A case of Mayer-Rokitansky-Küster-Hauser syndrome presenting as Graves disease
-
Ye-Jee Lim
,
Seung-Hun Kang
Published/Copyright:
October 25, 2012
Abstract
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder characterized by aplasia of the uterus and the upper part of the vagina in an XX individual with normal development of secondary sexual characteristics. Individuals with this syndrome may also present with renal and skeletal abnormalities. We report a case of a 16-year-old girl presenting with thyrotoxicosis and primary amenorrhea. After being diagnosed with Graves disease, this patient was placed on antithyroid medication. Although her thyroid function normalized, she did not start to menstruate. Therefore, we assessed her primary amenorrhea and diagnosed the patient with MRKH syndrome through pelvic imaging. To our knowledge, an association between Graves disease and MRKH syndrome has not yet been reported.
Keywords: Mayer-Rokitansky-Küster-Hauser syndrome; Müllerian aplasia; primary amenorrhea; thyrotoxicosis
Received: 2012-6-11
Accepted: 2012-6-25
Published Online: 2012-10-25
Published in Print: 2012-12-01
©2012 by Walter de Gruyter Berlin Boston
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Keywords for this article
Mayer-Rokitansky-Küster-Hauser syndrome;
Müllerian aplasia;
primary amenorrhea;
thyrotoxicosis
Articles in the same Issue
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- Review article
- The pros and cons of sex steroid priming in growth hormone stimulation testing
- Images in pediatric endocrinology
- Tuber sinerium hamartoma causing precocious puberty in a child
- Original articles
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- Disorders of sex development among Sudanese children: 5-year experience of a pediatric endocrinology clinic
- Anti-Müllerian hormone levels in serum 1 year after unilateral orchiopexy
- Clinical and genetic analysis of three Chinese patients with steroid 5α-reductase type 2 deficiency
- Apparent mineralocorticoid excess syndrome: report of one family with three affected children
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- Acanthosis nigricans predicts the clustering of metabolic syndrome components in Hispanic elementary school-aged children
- Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy
- Increased endothelial microparticles in obese and overweight children
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