- Glucose-6-phosphate Dehydrogenase Deficiency
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Lee JM
- KMID: 2168913
- Clin Pediatr Hematol Oncol.
- 2015 Apr;22(1):1-7.
- doi: 10.15264/cpho.2015.22.1.1
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder. There are more than 400 million people worldwide with G6PD deficiency, and its distribution is similar to that of malaria.... -
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- Jaundice and Hemolytic Anemia Appearing within the First 24 Hour of Life due to Glucose-6-Phosphate Dehydrogenase Deficiency
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Kim KM, Lee JH, Chun CS
- KMID: 1876165
- Korean J Perinatol.
- 2006 Mar;17(1):89-93.
The most devastating clinical consequence of G-6-PD deficiency is neonatal hyperbilirubinemia which can be severe and result in kernicterus or even death, although glucose-6-phosphate dehydrogenase deficiency is responsible for two... -
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- Anesthetic management of a patient with glucose-6-phosphate dehydrogenase deficiency undergoing robot-assisted laparoscopic surgery: A case report
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Cho H, Lee SY, Kim GH, Kim J, Koo MS, Yun M, Kwon MY
- KMID: 2388840
- Anesth Pain Med.
- 2017 Jul;12(3):243-246.
- doi: 10.17085/apm.2017.12.3.243
The authors describe the successful perioperative management of a 3-year-old boy from Dubai with glucose-6-phosphate dehydrogenase (G6PD) deficiency, who underwent robot-assisted laparoscopic pyeloplasty for complete right ureteropelvic junction obstruction. G6PD... -
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- Glucose-6-phosphate dehydrogenase deficiency: report of 4 cases
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Kim MK, Yang CH, Kang SH, Lyu CJ, Kim KY
- KMID: 1421894
- J Korean Med Sci.
- 1992 Mar;7(1):71-75.
- doi: 10.3346/jkms.1992.7.1.71
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary enzyme disorder and more than 200 million people have a deficiency in this enzyme. It is a globally important cause... -
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- Hypohidrotic Ectodermal Dysplasia Associated with Glucose-6-Phosphate Dehydrogenase Deficiency
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Ermertcan , Yasar A, Kayhan TC, Gulen H, Ertan P
- KMID: 2156740
- Ann Dermatol.
- 2011 Sep;23(Suppl 1):S8-S10.
- doi: 10.5021/ad.2011.23.S1.S8
Hypohidrotic ectodermal dysplasia (HED) is a syndrome characterized by hypodontia, hypotrichosis, and partial or total ecrine sweat gland deficiency. The most prevalent form of HED is inherited as an X... -
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- Acute Hemolysis and Renal Failure caused by Hepatitis A Infection with Underlying Glucose-6-Phosphate Dehydrogenase Deficiency
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Jekarl DW, Oh EJ, Park YJ, Han KJ, Lee SW, Park CW
- KMID: 1781482
- Korean J Lab Med.
- 2007 Jun;27(3):188-191.
- doi: 10.3343/kjlm.2007.27.3.188
Although glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder worldwide, it has rarely been reported among Korean. The patient was previously healthy 39 yr old male who showed... -
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- A Case of Glucose-6-Phosphate Dethydrogenase Deficiency with Chronic Hepatitis B
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Choi JA, Kim SY, Lee W, Lee BC, Shu BK
- KMID: 2193920
- J Korean Soc Pediatr Endocrinol.
- 1998 May;3(1):90-95.
Glucose-6-phosphate dehydrogenase(G6PD) deficiency is the most common X- linked inherited disorder and is estimated to affect 400 million people worldwide. But the incidence of this disease is very rare in... -
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- Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency
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Isa HM, Mohamed MS, Mohamed AM, Abdulla A, Abdulla F
- KMID: 2377098
- Korean J Pediatr.
- 2017 Apr;60(4):106-111.
- doi: 10.3345/kjp.2017.60.4.106
PURPOSE: This study aimed to determine the prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency among infants with neonatal indirect hyperbilirubinemia (NIH); compare G6PD-deficient and G6PD-normal patients regarding hyperbilirubinemia and need for... -
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- Glucose-6-phosphate dehydrogenase deficiency does not increase the susceptibility of sperm to oxidative stress induced by Hâ‚‚Oâ‚‚
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Roshankhah S, Rostami-Far Z, Shaveisi-Zadeh F, Movafagh A, Bakhtiari , Shaveisi-Zadeh J
- KMID: 2364655
- Clin Exp Reprod Med.
- 2016 Dec;43(4):193-198.
- doi: 10.5653/cerm.2016.43.4.193
OBJECTIVE: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect. G6PD plays a key role in the pentose phosphate pathway, which is a major source of nicotinamide adenine... -
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- Red Blood Cell Enzymopathies Causing Hereditary Hemolytic Anemia
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Hah JO
- KMID: 1441716
- Clin Pediatr Hematol Oncol.
- 2012 Apr;19(1):1-6.
The RBC enzyme deficiencies causing hereditary hemolytic anemia (HHA) can be divided into three groups: those participating in the glycolytic (E-M) pathway; those involved with the maintenance of a high... -
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- Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase Deficiency
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Lee J, Park J, Choi H, Kim J, Kwon A, Jang W, Chae H, Kim M, Kim Y, Lee JW, Chung NG, Cho B
- KMID: 2373627
- Ann Lab Med.
- 2017 Mar;37(2):108-116.
- doi: 10.3343/alm.2017.37.2.108
BACKGROUND: We describe the genetic profiles of Korean patients with glucose-6-phosphate dehydrogenase (G6PD) deficiencies and the effects of G6PD mutations on protein stability and enzyme activity on the basis of... -
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- Pityriasis Rotunda Associated with Hepatocellular Carcinoma
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Jeong YI, Lee DK, Chang SE, Lee MW, Choi JH, Moon KC, Koh JK
- KMID: 2158512
- Ann Dermatol.
- 2004 Mar;16(1):42-44.
- doi: 10.5021/ad.2004.16.1.42
Pityriasis rotunda is an unusual disease characterized by perfectly circular or oval-shaped dyschromic patches with a scaling surface. Histologically, the lesions resemble those of ichthyosis vulgaris. They typically involve the... -
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- Tosufloxacin Tosylate Increased the Liver Enzyme Levels in a Bladder Cancer Patient with Normal Liver Functions: a Case Report
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Choi EJ, Song IJ, Rhew KY, Yoon H
- KMID: 2226402
- Korean J Clin Pharm.
- 2015 Mar;25(1):56-58.
- doi: 10.0000/kjcp.2015.25.1.56
SUMMARY: We report the first hepatic adverse effect of tosufloxacin tosylate in a muscle invasive bladder cancer patient with normal liver functions and with scheduling to undergo a surgical operation... -
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