- A case of sirenomelia in a FDIU at 28 week
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Kim IH, Park JK, Jang SR, Hwang BS
- KMID: 2259779
- Korean J Obstet Gynecol.
- 1993 Jul;36(7):3171-3175.
No abstract available. -
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- A case of sirenomelia
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Kim HK, Jung HS, Lee SK, Suh BH, Lee JH
- KMID: 1696927
- Korean J Obstet Gynecol.
- 1992 May;35(5):774-777.
No abstract available. -
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- A Case of Sirenomelia
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Kim HK, Cho SI, Kim BT, Cha HJ, Lee SJ
- KMID: 1683222
- J Korean Pediatr Soc.
- 1990 Feb;33(2):241-245.
No abstract available. -
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- A case of sirenomelia
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Yoo JH, Park MI, Chung SR, Lee JA, Kim NH, Hong EK
- KMID: 1691527
- Korean J Perinatol.
- 1993 Sep;4(3):415-421.
No abstract available. -
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- A Case of Sirenomelia
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Chao MC, Lee SJ, Jo JS, Kim HS, Moon DS, Cho CD
- KMID: 1676523
- J Korean Pediatr Soc.
- 1986 Mar;29(3):100-103.
No abstract available. -
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- Poland's Syndrome: Report of a Case
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Lee BK, Kim JH, Jung SH
- KMID: 2006618
- J Korean Breast Cancer Soc.
- 2003 Jun;6(2):127-130.
- doi: 10.4048/jkbcs.2003.6.2.127
Poland's syndrome is characterized by hypoplasia or absence of the breast of nipple, hypoplasia of subcutaneous tissue, absence of the costosternal portion of the pectoralis major muscle, absence of the... -
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- Amelia of Both Lower Extremities: A Case Report
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Lim JS, Kim YS, Pyun YS, Kang CS, Kim ID
- KMID: 2463938
- J Korean Orthop Assoc.
- 1972 Dec;7(4):477-480.
- doi: 10.4055/jkoa.1972.7.4.477
A case of amelia, which affected upon both lower extremities, was experienced at the Taegu Presbyterian Hospital. We report this case because of rarity of amelia and an addition of... -
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- A case of Roberts syndrome
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Choi Y, Chung YH, Lim IS, Kim CH, Lee DK, Kim SN, Song SY, Chi JG
- KMID: 2042044
- J Korean Pediatr Soc.
- 1993 Oct;36(10):1447-1451.
Roberts syndrome is an autosomal recessive disorder accompanied by limb defects, craniofacial abnormalities, pre-and postnatal growth retardation. Patients with Roberts syndrome have characteristic premature separation of heterochromatin of many chromosomes... -
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- Fibular Hemimelia: A Case Report
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Kim BJ, Hong SJ, Kim KM, Seol HY, Cha IH, Song HR
- KMID: 2024471
- J Korean Radiol Soc.
- 2006 Nov;55(5):505-509.
- doi: 10.3348/jkrs.2006.55.5.505
Fibular hemimelia is the most common congenital absence or hypoplasia of long bone. In addition to fibular absence or hypoplasia, this entity also includes various combined abnormalities of the lower... -
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- Caudal Regression Syndrome: A Case Report
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Lee EJ, Kim JH, Kim HS, Park SY, Han HY, Lee KH
- KMID: 2377159
- J Korean Radiol Soc.
- 1998 Jul;39(1):181-184.
Caudal regression syndrome is a rare congenital anomaly, which results from a developmental failure of thecaudal mesoderm during the fetal period. We present a case of caudal regression syndrome composed... -
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- A case of sirenomelia diagnosed after amnioinfusion
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Yoon J, Yoon ES, Kim MR, Koo BS, You HJ, Kim YM, Cha HJ, Lee HW
- KMID: 2272549
- Korean J Obstet Gynecol.
- 2005 Feb;48(2):451-456.
Sirenomelia, also known as the mermaid syndrome, is a rare and usually lethal congenital malformation of uncertain etiology. It is characterized by fusion of the lower limbs and commonly associated... -
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- A Case of Sirenomelia Diagnosed at 12 Gestational Weeks
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Song GY, Han SS, Kim YH, Gwon HG, Lee CH, Jo JS, Park YW
- KMID: 2262198
- Korean J Obstet Gynecol.
- 2001 Jan;44(1):198-201.
Sirenomelia, characterised by a complete or incomplete fusion of the lower extremities, is a severe form of caudal defect affecting 1.5-4.2 in 100,000 births. Most cases of sirenomelia die within... -
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- A Case of Sirenomelia Diagnosed at 14 Gestational Weeks
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Jeong EH, Kong DS, Kim IH, Lee KS, Lee GH, Kim JH, Kim SJ
- KMID: 1838162
- Korean J Perinatol.
- 2003 Dec;14(4):422-426.
Sirenomelia, characterised by a complete or incomplete fusion of the lower extremities, is a severe form of caudal defect affecting 1 in 60,000 births. Most cases of sirenomelia die within... -
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- A Case of Sirenomelia without Oligohydramnios Diagnosed in Early Second Trimester
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Park HJ, An HS, Kim JE, Lee SA, Choi KA, Jeong SJ, Chi WY
- KMID: 1876166
- Korean J Perinatol.
- 2006 Mar;17(1):94-98.
Sirenomelia is rare congenital malformation characterized by fusion of the lower extrimities associated anomalies included absence of urogenital system (bilateral renal agenesis, absent ureter, urinary bladder, absent internal and external... -
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- A Case of VATER association Variant with a 46, XY, inv (6)(q11q16) Inversion
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Park DH, Jung DB, Yang ES, Park YB, Park SK
- KMID: 2207973
- J Korean Pediatr Soc.
- 1998 Mar;41(3):396-400.
VATER association of vertebral defects, imperforate anus, tracheoesophageal (T-E) fistula with esiphageal atresia, and radial and renal dysplasia are utilized to identify this complex. Other anomalies are vascular anomalies (cardiac... -
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- Radial nerve injury due to automatic blood pressure monitoring: A case report
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Kim YS, Kwak KH, Hong JG
- KMID: 2238093
- Korean J Anesthesiol.
- 2009 Aug;57(2):217-220.
- doi: 10.4097/kjae.2009.57.2.217
We experienced an unusual complication of acute radial nerve palsy presenting as wrist drop after application of automated cycled blood pressure monitoring for 3 hours. A 19-year-old ASA physical status... -
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- A Case of Sirenomelia In One Fetus of Twin Pregnancy
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Jung SG, Kim HC, Kim YS, Kim YA, Kim JY, Kim JY, Shin SJ, Kim NK, Kang HY, Park JS
- KMID: 2272321
- Korean J Obstet Gynecol.
- 2004 Apr;47(4):789-794.
Sirenomelia is a lethal congenital malformation characterized by single or fused lower limbs associated with other severe genitourinary and lower gastrointestinal tract anomalies. Associated anomalies include malformation of vertebrae and... -
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- Analysis of FUDR --induced Congenital Anomalies in the Rat
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Yang EJ, Choi SP, Cho KJ, Kim SI, Kwon OY, Lee YH, Kim WS
- KMID: 2283034
- Korean J Phys Anthropol.
- 1997 Dec;10(2):191-198.
For the study on the teratogenic effects and its mechanism of FUDR on the developing rat fetuses, Sprague -Dawley rats as experimental animal and 5 -fluoro -2 '-deoxyuridine (Sigma chemicals)... -
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- Phocomelia: The Clinical Manifestation, Classification and Surgical Treatment of Korean Patients with Phocomelia
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Baek GH, Chung MS, Lee YH, Gong HS, Rhee SH, Kim JY, Lee SJ
- KMID: 2336164
- J Korean Orthop Assoc.
- 2008 Dec;43(6):685-693.
PURPOSE: Phocomelia is an extremely rare congenital anomaly of the upper extremity. There have been no clinical reports about phocomlia in Korea except for five birth reports. We present here... -
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