- A Case of Prader Willi syndrome
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No authors listed
- KMID: 1691294
- J Korean Pediatr Soc.
- 1992 May;35(5):678-683.
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- One Case of the Prader-Willi Syndrome
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Choi WS, Kim KB, Ryoo HS, Lee SH, Kim KS
- KMID: 2139712
- Korean J Urol.
- 1981 Dec;22(6):630-632.
Prader-Willi syndrome is characterized by such as infantile hypotonia, mental retardation hyperphagia with obesity and hypogonadism. We experienced one case of so called Prader-Willi syndrome associated with hypogonadotrophic hypogonadism, hypomentia,... -
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- Ghrelin in the Prader-Willi Syndrome
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Jin DK
- KMID: 1515000
- J Korean Soc Pediatr Endocrinol.
- 2003 Dec;8(2):119-125.
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- Prader-Willi Syndrome with Hypogonadism
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Lee GH
- KMID: 2298630
- Korean J Androl.
- 2011 Apr;29(1):85-87.
- doi: 10.5534/kja.2011.29.1.85
Prader-Willi syndrome (PWS) is a rare genetic disease caused by a deletion or disruption of genes in chromosome 15. Commonly associated characteristics of this disorder include obesity, mental retardation, short... -
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- A Case of Prader-Willi Syndrome
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Soung YM, Shin YS, Shin MJ, Kang SC
- KMID: 1946130
- J Korean Pediatr Soc.
- 1980 Jul;23(7):590-597.
Prader-Willi syndrome is characterized by 1) hypotonia in the newborn infant 2) obesity which begins in childhood 3) short stature 4) typical facial features 5) secondary hypogonadism 6) juvenile diabetes... -
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- Experience of severe desaturation during anesthetic induction period in an obese adult patient with Prader-Willi syndrome: A case report
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Choi JW, Kim EJ, Min BW, Ban JS, Lee SG, Lee JH
- KMID: 2236300
- Korean J Anesthesiol.
- 2012 Feb;62(2):179-183.
- doi: 10.4097/kjae.2012.62.2.179
Prader-Willi syndrome is characterized by infantile hypotonia, childhood-onset obesity, short stature, mental retardation, hyperphagia, hypogonadism. After infantile hypotonia phase, patient is prone to morbid obesity due to hyperphagia. Complications associated... -
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- A Case of Prader-Willi Syndrome with Diabetes Mellitus
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Choi HR, Choi EH, Jang SH, Ahn YM
- KMID: 2335114
- J Korean Pediatr Soc.
- 1994 Apr;37(4):565-572.
Prader-Willi syndrome is characterized by infantile hypotonia, mental retardation, hyperhagia, hypogonadism and obesity. Approximately 60% of all PLW syndrome show an interstitial deletion of chromosome 15, 37% have apparently normal... -
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- Focal Segmental Glomerulosclerosis in a Child with Prader-Willi Syndrome: A Case of Obesity-associated Focal Segmental Glomerulosclerosis
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Cho HY, Chung DL, Kang JH, Ha IS, Cheong HI, Choi Y
- KMID: 2098820
- J Korean Soc Pediatr Nephrol.
- 2004 Oct;8(2):244-249.
Obesity-associated focal segmental glomerulosclerosis(OB-FSGS) has been known to progress into advanced renal insufficiency, and its clinicopathological features include obesity, FSGS lesions with glomerulomegaly and, nephrotic-range proteinuria without edema. A 14-... -
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- Clinical Usefulness of Aripiprazole Treatment in a Girl with Prader-Willi Syndrome and Psychosis
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Briegel W
- KMID: 2428980
- Clin Psychopharmacol Neurosci.
- 2018 Nov;16(4):497-500.
- doi: 10.9758/cpn.2018.16.4.497
Prader-Willi syndrome (PWS) is a quite rare multi-systemic genetic disorder strongly associated with psychiatric illness in adults, especially psychosis. This report presents a 16-year-old female with PWS and symptoms of... -
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- Anesthetic Management in Pediatric Patient with Prader-Willi Syndrome: A case report
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Min SH, Lim CH, Lee HW, Lim HJ, Yoon SM, Chang SH
- KMID: 2299118
- Korean J Anesthesiol.
- 2004 Sep;47(3):439-441.
- doi: 10.4097/kjae.2004.47.3.439
Prader-Willi syndrome is brought by chromosomal abnormality and is characterized by mental retardation, morbid obesity, infantile hypotonia, hypogenitalism. While feeding problems arise during infancy due to hypotonia, it is followed... -
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- Prader-Willi Syndrome: A case report
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Cho EC, Jee SE, Jang Y, Park SS, Kim JT, Song HK
- KMID: 2238624
- Korean J Anesthesiol.
- 1999 Jun;36(6):1091-1094.
- doi: 10.4097/kjae.1999.36.6.1091
In 1956, Prader and Willi first described a clinical syndrome that included severe neonatal hypotonia, hyperphagia, obesity, diabetes, hypogonadism, cryptorchidism, dental caries and mental deficiency. We have anesthetized a male... -
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- A Case of Prader-Willi Syndrome with FUO Diagnosed at Infancy
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Kim JH, Jeong JH, Cho SM
- KMID: 2207507
- J Korean Pediatr Soc.
- 2000 Aug;43(8):1142-1148.
Prader-Willi syndrome(PWS) was first described by Prader et al in 1956. This syndrome is characterized by diminished fetal activity, low birth weight, infantile hypotonia with feeding problem, temperature instability, early onset of... -
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- The Usefulness of Fluorescence in Situ Hybridization(FISH) in the Diagnosis of Prader-Willi Syndrome
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Yang YH, Kim DH, Chung SC, Sohn YS, Kim MS
- KMID: 2335473
- J Korean Pediatr Soc.
- 2000 Mar;43(3):360-364.
PURPOSE: To detect microdeletion of 15q11-13 region, high resolution cytogenetic analysis or FISH with probe at Prader-Willi syndrome region can be used. We tried to evaluate whether FISH with SNRPN... -
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- A Case of Prader-Willi Syndrome with Bilateral Hutch Diverticula Associated with Vesicoureteral Reflux
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Han SJ, Lee JE, Lee T, Kim WH, Hong YJ, Jun YH
- KMID: 1853430
- J Korean Soc Pediatr Nephrol.
- 2005 Apr;9(1):112-116.
Our patient is the first reported case of Prader-Willi syndrome(PWS) with bilateral Hutch's diverticula. We believe that hypotonia in PWS is associated with multiple bladder diverticula and vesicoureteral reflux. We... -
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- Experience with reversal of a neuromuscular block with sugammadex in a child with Prader-Willi syndrome: A case report
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Sung TY, Kang T, Cho CK, Kwon HU, Kang PS, Jee YS
- KMID: 2405850
- Anesth Pain Med.
- 2017 Oct;12(4):335-338.
- doi: 10.17085/apm.2017.12.4.335
We treated a 4-year-old patient with a genetic disorder, Prader-Willi syndrome, that was accompanied by pulmonary hypertension due to upper airway obstruction. Prader-Willi syndrome is a complex genetic condition characterized... -
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- Leptin Levels and Obesity in Childhood
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Chung SC, Kim DH
- KMID: 2193799
- J Korean Soc Pediatr Endocrinol.
- 1999 Dec;4(2):211-218.
PURPOSE: Leptin is a hormone involved in the regulation of energy balance. Serum leptin levels are correlated with body fat. It provide information to hypothalamus on the amount of energy... -
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- Molecular Diagnostic Test for Prader-Willi Syndrome with SNRPN Expression
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Chung SC, Kim DH, Hong CH
- KMID: 2193801
- J Korean Soc Pediatr Endocrinol.
- 1999 Dec;4(2):226-230.
PURPOSE: Prader-Willi Syndrome(PWS) is caused by absence of paternal contributions of the chromosome region 15q11-q13. To detact this region, high resolutional cytogenetic analysis, FISH with probe at PWS critical region... -
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- Anesthetic management in a pediatric patient with infantile phase Prader-Willi Syndrome: A case report
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Kim JY, Lee JH, Kim EJ, Lee SK, Ban JS, Min BW
- KMID: 2238103
- Korean J Anesthesiol.
- 2009 Aug;57(2):259-263.
- doi: 10.4097/kjae.2009.57.2.259
Prader-Willi syndrome is a genetic disorder characterized by infantile hypotonia, childhood obesity, characteristic facial appearance, mental retardation, hypogonadism and short stature. It is described as a 2-stage disorder with an... -
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- Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
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Cheon CK
- KMID: 2366787
- Ann Pediatr Endocrinol Metab.
- 2016 Sep;21(3):126-135.
- doi: 10.6065/apem.2016.21.3.126
The Prader-Willi syndrome (PWS) is a human imprinting disorder resulting from genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. This genetic condition appears to be... -
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- General anesthetic management of Prader-Willi syndrome patient undergoing middle cerebral artery-superficial temporal artery anastomosis
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Lee JY, Cho KR, Kim MH, Lee KM, Kim HJ
- KMID: 2092347
- Korean J Anesthesiol.
- 2012 Jul;63(1):85-86.
- doi: 10.4097/kjae.2012.63.1.85
No abstract available. -
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