- Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report
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Jeong GH, Park BS, Jeong TK, Ma SK, Yeum CH, Kim SW, Kim NH, Choi KC
- KMID: 2157637
- J Korean Med Sci.
- 2003 Apr;18(2):284-286.
- doi: 10.3346/jkms.2003.18.2.284
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases... -
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- Clinical Characteristics of Renal Transplant Recipients that Underwent Urologic Surgery for de novo Disease Before and After Transplantation
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Bae KS, Huh JS, Kim YJ, Chang SG
- KMID: 1781729
- J Korean Med Sci.
- 2005 Feb;20(1):75-78.
- doi: 10.3346/jkms.2005.20.1.75
The pre-transplantation goal of the urologist is the optimization of urinary tract condition. Therefore, urologic surgery may be needed before or after renal transplantation. We analyzed the results of urologic... -
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- Magnetic Resonance Evaluation of Mullerian Remnants in Mayer-Rokitansky-Kuster-Hauser Syndrome
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Yoo RE, Cho JY, Kim SY, Kim SH
- KMID: 1482782
- Korean J Radiol.
- 2013 Apr;14(2):233-239.
- doi: 10.3348/kjr.2013.14.2.233
OBJECTIVE: To analyze magnetic resonance imaging (MRI) findings of Mullerian remnants in young females clinically suspected of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome in a primary amenorrhea workup. MATERIALS AND METHODS: Fifteen young females... -
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- Hysteroscopic Resection of the Vaginal Septum in Uterus Didelphys with Obstructed Hemivagina: A Case Report
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Kim TE, Lee GH, Choi YM, Jee BC, Ku SY, Suh CS, Kim SH, Kim JG, Moon SY
- KMID: 1127104
- J Korean Med Sci.
- 2007 Aug;22(4):766-769.
- doi: 10.3346/jkms.2007.22.4.766
Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis is a rare congenital anomaly. Excision of the obstructed vaginal septum is the treatment of choice for symptom relief and the... -
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- The First Korean Case of HDR Syndrome Confirmed by Clinical and Molecular Investigation
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Cheon CK, Kim GH, Yoo HW
- KMID: 2352821
- Yonsei Med J.
- 2015 Jan;56(1):300-303.
- doi: 10.3349/ymj.2015.56.1.300
Hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is a rare condition inherited as autosomal dominant trait and characterized by hypoparathyroidism, sensorineural deafness, and renal dysplasia. HDR syndrome is caused by... -
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