- A Case of Arthrogryposis Multiplex Congenita
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Lee YD, Joo AE, Kim HS, Yang JI, Chang KH, Oh KS
- KMID: 1925237
- Korean J Obstet Gynecol.
- 1997 Nov;40(11):2585-2589.
A case of arthrogryposis multiplex congenita is an extremely rare and complex syndrome characterized by contractures of multiple joints in different parts of the body. Arthrogryposis multiplex congenita usually occurs... -
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- A case of arthrogryposis multiplex congenita
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Lee JM, Kim SM, Nam HK, No JS
- KMID: 1691150
- J Korean Pediatr Soc.
- 1992 Jun;35(6):834-839.
No abstract available. -
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- Arthrogryposis Multiplex Congenita
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- KMID: 2461283
- J Korean Orthop Assoc.
- 1976 Sep;11(3):403-413.
- doi: 10.4055/jkoa.1976.11.3.403
No abstract available. -
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- A clinical study on arthrogryposis multiplex congenita
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Lee SH, Suh SW, Moon JY, Hong JS
- KMID: 1691077
- J Korean Orthop Assoc.
- 1993 Oct;28(6):2290-2295.
No abstract available. -
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- A Case of Arthrogryposis Multiplex Congenita in Identical Twin
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An CI, Min BG, Cho KS, Jo JD
- KMID: 1683631
- J Korean Pediatr Soc.
- 1990 Oct;33(10):1429-1433.
No abstract available. -
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- Arthrogryposis Multiplex Congenita in Siblings
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Choi KH, Park JA, Kim KS, Kim KB
- KMID: 1661206
- J Korean Pediatr Soc.
- 1995 Sep;38(9):1293-1298.
No abstract available. -
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- A Case of Arthrogryposis Multiplex Congenita
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Kee SS, Hwang SK, Choo BI, Yun HG, Lee HS, Oh SJ
- KMID: 1676521
- J Korean Pediatr Soc.
- 1986 Mar;29(3):90-94.
No abstract available. -
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- A Case of ARC (Arthrogryposis, Renal dysfunction and Cholestasis) Syndrome with a Dead Sibling Presenting Cholestatic Jaundice
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Choi HA, Lee JH, Chun CS
- KMID: 2144530
- J Korean Soc Neonatol.
- 2007 May;14(1):103-108.
A case of ARC syndrome was found in a newborn male with persistent cholestasis. He showed renal dysfunction, failure to thrive, and ichthyosis as well as arthrogryposis. The patient who... -
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- Two Cases of ARC (Arthrogryposis, renal dysfunction and cholestasis) Syndrome
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Hong JH, Lee CH, Chung KS
- KMID: 2275127
- Korean J Pediatr Gastroenterol Nutr.
- 2000 Mar;3(1):110-115.
ARC (arthrogryposis multiplex congrnita, renal dysfunction and cholestasis) syndrome was first described by Lutz-Richner and Landolt in 1973 and after then similar cases were scarcely reported worldwide. There's no reported... -
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- A Card of Arthrogryposis Multiplex Congenita with Congenital Hypertropic Pyloric Stenosis
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Yang SC, Kim SY, Kim HH, Han SH, Byun JI, Lee WB
- KMID: 2208297
- J Korean Pediatr Soc.
- 1995 Nov;38(11):1577-1582.
No abstract available. -
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- A Case of Arthrogryposis Multiplex Congenita Diagnosed by Prenatal Ultrasonography
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Kim SY, Gil MK, Kang YM, Jeong SJ, Kim YN, Jeong DH, Lee KB, Sung MS, Kim KT
- KMID: 2077534
- Korean J Obstet Gynecol.
- 2005 Dec;48(12):2966-2970.
Arthrogryposis multiplex congenita is congenital disorder that characterized by multiple joint contractures. Although there are characteristic morphologic features, most of cases are diagnosed at birth and cases diagnosed by prenatal... -
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- Anesthesia in patients with arthrogryposis multiplex congenita: a report of 10 patients
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Jung JW, Heo BY, Oh EJ, Chung YH
- KMID: 1738836
- Korean J Anesthesiol.
- 2014 Dec;67(Suppl):S89-S90.
- doi: 10.4097/kjae.2014.67.S.S89
No abstract available. -
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- A case of arthrogryposis multiplex congenita associated with maternal septate uterus
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Kim HK, Oh HK, Hong SY
- KMID: 2274141
- Korean J Obstet Gynecol.
- 2012 Sep;55(9):669-672.
- doi: 10.5468/KJOG.2012.55.9.669
Arthrogryposis multiplex congenita (AMC) is a congenital disorder showing multiple joint contractures. Although there are characteristic features in morphology, it is difficult to diagnose prenatally by ultrasonography. The causes of... -
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- Amyoplasia Congenita of the Lower Extremity: Report in a Premature Baby
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Lee HS
- KMID: 1716529
- Yonsei Med J.
- 2005 Aug;46(4):567-570.
- doi: 10.3349/ymj.2005.46.4.567
Amyoplasia congenita is a diagnostic subgroup of children with arthrogryposis multiplex congenita (AMC). AMC is a relatively rare syndrome characterized by multiple joint contractures at birth. Amyoplasia congenita is the... -
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- Factors Affecting Recurrence After Soft Tissue Release for Talipes Equinovarus in Arthrogryposis Multiplex Congenita
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Kim SB, Cho TJ, Choi IH, Chung CY, Ahn JH, Lee DY
- KMID: 2336102
- J Korean Orthop Assoc.
- 1998 Oct;33(5):1379-1384.
Talipes equinovarus deformity associated with arthrogryposis multiplex congenita(AMC) is rigid and its treatment is still controversial. The purpose of this study is to review the trend of recurrence after soft... -
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- A Case of Escobar Syndrome (Multiple Pterygium Syndrome)
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Kim GH, Kim JY, Song ES, Woo YJ, Choi YY
- KMID: 2188598
- J Korean Soc Neonatol.
- 2006 May;13(1):189-193.
Multiple pterygium (Escobar) syndrome is a rare disorder manifested by growth retardation, facial and genital anomalies, and widespread musculo-skeletal deformities. This disorder was originally described by Bussiere in 1902. And... -
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- A Case of Partial Short Arm Deletion in Chromosome 9 with Inguinal Hernia, Testicular Cystic Lesion, and Arthrogryposis Multiplex Congenita
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Kim EJ, Chung SH, Park TS, Choi YS
- KMID: 2379660
- Neonatal Med.
- 2017 May;24(2):88-91.
- doi: 10.5385/nm.2017.24.2.88
Chromosome 9p syndrome is a rare chromosomal abnormality caused by a partial deletion in chromosome 9. It was first described in 1973 by Alfi et al., and has since been... -
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- A Case of 13q- Syndrome with Arthrogryposis Multiflex Congenita
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Ko YS, Kim MS, Choi SI, Cho SC
- KMID: 2188694
- J Korean Soc Neonatol.
- 2003 May;10(1):103-107.
13q- syndrome is a rare genetic disorder characterized by psychomotor retardation, hypotonia, microcephaly, retinoblastoma, ptosis and coloboma. Facial and congenital heart anomalies are also found and about 60% of males... -
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- A Case of Neonatal Cholestasis with Arthrogryposis Multiplex Congenita and Renal Tubular Insufficiency(ARC Syndrome)
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Rhee HS, Kim SY, Baik NS, Ha IS, Seo JK
- KMID: 2335169
- J Korean Pediatr Soc.
- 1996 Jan;39(1):126-130.
We report a case of ARC syndrome with arthrogryposis multiplex congenita, renal tubular insufficiency and cholestasis. The Patient presented in the early neonatal period with micrognathia, low set ears,... -
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- A Case of Congenital Hyperextension of the Knee
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Lee SC, Kim HI, Baek SH, Kim KS
- KMID: 1838617
- J Korean Soc Neonatol.
- 1998 Jun;5(1):72-76.
Congenital dislocation of the knee is a very rare condition and was first described by Chatelaine in 1822. The etiology of this condition is unknown. It is generally subclassified as... -
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