- A Case of Beckwith-Wiedemann Syndrome
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No authors listed
- KMID: 1691994
- J Korean Pediatr Soc.
- 1991 Jan;34(1):126-129.
No abstract available. -
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- Beckwith-Wiedemann Sydrome with Left Adrenal Cortical Neoplasm
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Jung JH, Ko JK, Song YT
- KMID: 2422161
- J Korean Assoc Pediatr Surg.
- 2000 Dec;6(2):160-165.
- doi: 10.13029/jkaps.2000.6.2.160
Beckwith-Wiedemann syndrome presents with multisystemic patterns of congenital anomalies and macrosomia. This syndrome was independently described by Beckwith in 1963 and by Wiedemann in 1964. There is wide spectrum of... -
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- Testicular Yolk Sac Tumor in Beckwith-Wiedemann Syndrome
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Park BJ, Jeong IY, Ro DW, Kim DY, Park JS
- KMID: 1663291
- Korean J Urol.
- 1996 Dec;37(12):1417-1420.
The Beckwith-Wiedemann syndrome, which included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, have a substantially increased risk for the development of tumor. We report a case of testicular... -
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- Mesenchymal Hamartoma of the Liver in Beckwith-Wiedemann Syndrome: A Case Report
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Yoo SH, Park HJ, Cho SY, Kim CJ
- KMID: 1725945
- Korean J Pathol.
- 2002 Dec;36(6):425-428.
Beckwith-Wiedemann syndrome is a well-known overgrowth syndrome associated with the presence of a wide variety of anomalies and increased risk of cancers. Less frequently, benign neoplasms also develop. We report... -
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- A case of Beckwith-Wiedemann Syndrome
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Hwang NJ, Back SM, Choi YS, Soe SS, Yoon HK
- KMID: 1946001
- J Korean Pediatr Soc.
- 1990 Mar;33(3):373-379.
No abstract available. -
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- A Case of Beckwith-Wiedemann Syndrome
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Wook JW, Choi EY, Kim MS, Lee HS, Ahn YM
- KMID: 1682719
- J Korean Pediatr Soc.
- 1988 Dec;31(12):1685-1688.
No abstract available. -
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- A Case of Beckwith-Wiedemann Syndrome
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Hong HS, Lee HC, Lee OK, Lee MH
- KMID: 1677135
- J Korean Pediatr Soc.
- 1987 Oct;30(10):1166-1169.
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- Anesthetic management of children with Beckwith-Wiedemann syndrome : Two cases report
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Kim HJ, Kim JT, Kim HJ, Kim HS, Kim CS, Kim SD
- KMID: 1782600
- Korean J Anesthesiol.
- 2009 May;56(5):583-586.
- doi: 10.4097/kjae.2009.56.5.583
Beckwith-Wiedemann syndrome consists of various abnormalities, including macroglossia, visceromegaly, omphalocele, and neonatal hypoglycemia. These abnormalities frequently require operative correction and careful anesthetic management. Principal problems associated with anesthetic management in... -
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- A case of Beckwith-Wiedemann Syndrome
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Choi JS, Kim BH, Chon YS, Kwang HI, Choi YY, Hwang TJ
- KMID: 1946000
- J Korean Pediatr Soc.
- 1990 Mar;33(3):367-372.
No abstract available. -
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- Perioperative airway management of a patient with Beckwith-Wiedemann syndrome
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Tsukamoto , Hitosugi T, Yokoyama T
- KMID: 2366161
- J Dent Anesth Pain Med.
- 2016 Dec;16(4):313-316.
- doi: 10.17245/jdapm.2016.16.4.313
Airway obstruction in pediatric patients always poses a challenge for anesthesiologists. Beckwith-Wiedemann syndrome causes various abnormalities such as macroglossia and omphalocele. Patients with these abnormalities often need corrective surgeries. Management... -
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- A CASE OF TONGUE RESECTION IN MACROGLOSSIA AS A PRESENTATION OF BECKWITH-WIEDEMANN SYNDROME
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Ahn KY, Jang KS, Park DH, Hwang JB
- KMID: 2119323
- J Korean Soc Plast Reconstr Surg.
- 1997 Jan;24(1):199-204.
The Beckwith-Wiedemann syndrome, originally described by Beckwith in 1963 and Wiedemann in 1964, included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, severe hypoglycemia, abdominal wall defect, capillary nevus... -
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- Reduction glossectomy of macroglossia in beckwith-wiedemann syndrome : a case report
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Kim HK, Kim ES, Ko YK, Kim SG
- KMID: 1575609
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 2005 Nov;27(6):559-564.
Beckwith-Wiedemann syndrome is an autosomal dominant growth excess disorder, which occurs with a reported incidence of 1 in 13,700 to 1 in 17,000 live births. It constitutes a discrete... -
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- Genetic syndromes associated with overgrowth in childhood
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Ko JM
- KMID: 2266359
- Ann Pediatr Endocrinol Metab.
- 2013 Sep;18(3):101-105.
- doi: 10.6065/apem.2013.18.3.101
Overgrowth syndromes comprise a diverse group of conditions with unique clinical, behavioral and molecular genetic features. While considerable overlap in presentation sometimes exists, advances in identification of the precise etiology... -
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- Prenatal Sonographic Findings of Beckwith-Wiedemann Syndrome: A Case Report
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Yoon WS, Lee JY, Lee YH
- KMID: 1898360
- J Korean Soc Med Ultrasound.
- 2000 Mar;19(1):35-37.
The Beckwith-Wiedemann syndrome(BWS) is and unusual complex with variable clinical features. Major findings include defects in the abdominal wall, macroglossia and macrosomia. These features should be amenable to prenatal ultrasound... -
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- A Case of Beckwith-Wiedemann Syndrome that Could be Diagnosed by Antenatal Care
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Kim SK, Kim JA, Chang YP, Park JW, Hur EJ
- KMID: 2072351
- Korean J Perinatol.
- 2002 Mar;13(1):56-61.
Beckwith-Wiedemann syndrome(BWS) is a group of disorders having in common coexistence of a macrosomia, macroglossia, abdominal wall defects, visceromegaly, hypoglycemia in the neonatal period and embryonal cancers of infancy and... -
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- Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome
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Kim EN, Song DE, Yoon HM, Lee BH, Kim CJ
- KMID: 2465453
- J Pathol Transl Med.
- 2019 Mar;53(2):129-135.
- doi: 10.4132/jptm.2018.11.13
Patients with Beckwith-Wiedemann syndrome (BWS) are predisposed to developing embryonal tumors, with hepatoblastoma being the most common type. Our patient showed hemihypertrophy, macroglossia, and paternal uniparental disomy in chromosome 11... -
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- Genetic Diagnosis of Beckwith Wiedemann Syndrome using Methylation Specific PCR-RFLP Method
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Kim GH, Lee JJ, Choi SH, Lee JY, Lee BH, Yoo HW
- KMID: 2184478
- J Genet Med.
- 2010 Dec;7(2):133-137.
PURPOSE: Beckwith-Wiedemann syndrome (BWS) is an overgrowth malformation syndrome caused by a methylation abnormality at chromosome 11p15, consisting of two imprinting centers, BWSIC1 (IGF2, H19) and BWSIC2 (LIT1, KvDMR). This... -
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- Three Cases of Russell-Silver Syndrome in One of Twins Conceived by In Vitro Fertilization
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Cho HJ, Song ES, Kim YH, Song TB, Choi YY
- KMID: 1472013
- Korean J Perinatol.
- 2009 Sep;20(3):266-272.
In vitro fertilization (IVF) is a main option for the infertility treatment and its major concerns are the risk of multiple pregnancy, preterm delivery, intrauterine growth retardation (IUGR), and congenital... -
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- Genetic overgrowth syndrome: A single center's experience
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Cheon CK, Kim YM, Yoon JY, Kim YA
- KMID: 2435944
- J Genet Med.
- 2018 Dec;15(2):64-71.
- doi: 10.5734/JGM.2018.15.2.64
PURPOSE: Overgrowth syndromes are conditions that involve generalized or localized areas of excess growth. In this study, the clinical, molecular, and genetic characteristics of Korean patients with overgrowth syndrome were... -
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- Placental Mesenchymal Dysplasia Associated with a Fetal Unilateral Multicystic Dysplastic Kidney: A Case Report
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Ahn JW, Lee PR, Kim MG, Kim KR, Shim JY, Won HS, Kim A
- KMID: 2280812
- Korean J Perinatol.
- 2010 Jun;21(2):174-179.
Placental mesenchymal dysplasia (PMD) is a rare placental disorder that may coexist with a normal fetus but is frequently associated with fetal growth restriction, fetal demise, prematurity, and Beckwith-Wiedemann syndrome,... -
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