Mayer-Rokitansky-Küster-Hauser Syndrome with a Solitary Duplex Kidney and Anal Stenosis: Report of a Rare Case - 21/01/21
Abstract |
Background |
To date, only 23 cases of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome with duplex kidney have been reported. We present the first reported case of MRKH syndrome with solitary duplex kidney and anal stenosis.
Case: |
A 17-year-old Chinese girl presented with primary amenorrhea and fully developed secondary sex characteristics. Ultrasonography of the abdomen and pelvis revealed the absence of the right kidney, a left duplex kidney, and a primordial uterus. Surgery for anal stenosis was performed when she was 1 year of age. The patient had a normal 46, XX karyotype.
Le texte complet de cet article est disponible en PDF.Key Words : Mayer-Rokitansky-Küster-Hauser syndrome, Solitary duplex kidney, Anal stenosis
Plan
| The authors declare that they have no conflict of interest regarding the publication of this case report. |
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| Author contributions: YB drafted, edited, and finalized the manuscript and reviewed the literature. K-NZ confirmed the patient's diagnosis via abdominal and pelvic ultrasound. M-LL obtained patient data and drafted the manuscript. All authors read and approved the final manuscript. |
Vol 34 - N° 1
P. 77-79 - février 2021 Retour au numéro
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