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Congenital Hydrocolpos Mimicking a Mature Cystic Teratoma in the Pelvis

Chang MY

Neonatal hydrocolpos is a rare condition that involves fluid accumulation in the vagina. On diagnostic imaging, the dilated vagina, along with the compressed uterus, can simulate a mature cystic teratoma...
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A Case of Neonatal Hydrocolpos due to Vaginal Atresia

Jo YJ, Park JH, Kim SY

  • KMID: 2427283
  • J Korean Assoc Pediatr Surg.
  • 2001 Dec;7(2):166-169.
A 37-week gestation female neonatal infant presented with lower abdominal distension. Ultrasonography showed a hydrocolpos, measuring 8.3 cm x 6.9 cm x 6.1 cm in size and on perineal examination,...
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Clinical experience with persistent cloaca

Cho MJ, Kim TH, Kim DY, Kim SC, Kim IK

PURPOSE: Persistent cloaca is one of the most severe types of anorectal malformation. Appropriate initial drainage is difficult due to their various malformations and hydrocolpos or dilated urinary bladder. Corrective...
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A Case of Persistent Cloaca with Hydrocolpos

Lee JW, Kim SK, Cho JS, Jeon MJ, Roh JL, Lee HJ, Park KH, Koo JS, Cho SH, Han SJ

  • KMID: 2076696
  • Korean J Obstet Gynecol.
  • 2002 Sep;45(9):1641-1644.
Persistent cloaca is a very rare congenital anomaly with a single common perineal opening for the genital, urinary and gastrointestinal tracts, which arises from defects in the embryonal process of...
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Two Cases of Herlyn-Werner-Wunderlich Syndrome in Neonates and Adolescents with Hydrocolpos and Hematocolpometra

Park M, Jeon GH

The Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly that is characterized by the triad of uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis. It is often diagnosed in patient...
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An ectopic ureterocele diagnosed in interlabial mass

Jang TK, Lim SY, Bae JG, Chang HS, Park JC, Rhee JH, Kim JI

Interlabial mass in infant is not common. Because of similarity of symptoms and signs of those mass and less experience of gynecologist due to those rarity, differential diagnosis is not...
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Prenatal Sonographic Finding of A Case of Hydrometrocolpos

Kim MJ, Kim SJ, Lee SH, Lee HJ, Moon BH, Lee JH, Park CH, Lee GS, Shin JC, Kim SP

  • KMID: 2262678
  • Korean J Obstet Gynecol.
  • 2002 Mar;45(3):508-512.
Cloacal anomalies are very rare congenital malformations with the incidence of 1/50,000-250,000 births. Hydrocolpos involves the dilatation of the vagina due to obstruction of the genital tract, leading to accumulation...
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A Case of Persistent Cloaca Diagnosed by Prenatal Sonography

Kim KH, Oh KY, Cho YH, Lee JC, Lee BK, Rho JH, Hwang IT, Yang YS, Park JS

  • KMID: 2077127
  • Korean J Obstet Gynecol.
  • 2004 Aug;47(8):1577-1581.
Persistent cloaca is a very rare congenital anomaly with a single common perineal opening for the genital urinary and gastrointestinal tract, which is caused by abnormal formation of the urorectal...
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Thin Glomerular Basement Membrane Disease with Herlyn-Werner-Wunderlich Syndrome: Uterus Didelphys, Blind Hemivagina and Ipsilateral Renal Agenesis

Kim MS, Park YJ, Park YJ, Park NH, Song JS, Kim PK

  • KMID: 2322139
  • J Korean Soc Pediatr Nephrol.
  • 2007 Oct;11(2):299-305.
Herlyn-Werner-Wunderlich syndrome(HWWs) is a rare variant of Mullerian ductal anomalies characterized by the presence of a hemivaginal septum, a didelphic uterus, and ipsilateral renal agenesis. It usually presents after menarche...
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A case of McKusick-Kaufman syndrome

Son SH, Kim YJ, Kim ES, Kim EK, Kim HS, Kim BI, Choi JH

McKusick-Kaufman syndrome (MKS) is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos (HMC) and postaxial polydactyly (PAP). We report a case of a female child with MKS who was...
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Gene Expression Modulation in Rat Skeletal Muscle by Denervation-induced Atrophy

Wang KB, Ahn JM, Kim HT, Kim CM, Suh JT

  • KMID: 2199066
  • J Korean Orthop Res Soc.
  • 2008 Oct;11(2):84-91.
PURPOSE: To understand the modulation of genes by atrophy, differential expression of genes in normal and denervated skeletal muscle was investigated by DNA chip technology. MATERIALS AND METHODS: Sciatic nerve and...
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