• Title/Summary/Keyword: CheongHaeJin

Search Result 83, Processing Time 0.033 seconds

A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy

  • Kim, Jae Choon;Kim, Ye Kyung;Hyun, Hye Sun;Park, Eu Jin;Kang, Hee Gyung;Ha, Il Soo;Cheong, Hae Il
    • Childhood Kidney Diseases
    • /
    • v.21 no.1
    • /
    • pp.35-39
    • /
    • 2017
  • Azathioprine is commonly used as immunosuppressive therapy for various inflammatory diseases including chronic glomerulonephritis. Myelosuppression is a common side effect of azathioprine, resulting in the need for dose reduction. However, severe pancytopenia or alopecia is not often encountered. Here, we report a case of severe myelosuppression, and alopecia totalis that occurred after azathioprine treatment in a patient with IgA nephropathy. A 10-year-old boy with IgA nephropathy was treated with oral deflazacort and later with azathioprine. After 4 weeks, the patient complained of hair loss, and despite a dose reduction in azathioprine, he developed bone marrow suppression and alopecia totalis in two weeks. The blood indices and alopecia of the patient had returned to normal after azathioprine withdrawal and 3 consecutive doses of granulocyte colony-stimulating factor. We suggest that physicians remain vigilant to the side effects of azathioprine. Unusual hair loss after azathioprine treatment might suggest a defect in the metabolism of the drug, warranting the discontinuation of azathioprine to prevent more severe side effects.

Two siblings with Bardet-Biedl syndrome caused by mutations in BBS10 : the first case identified in Korea

  • Yoon, Sung Chul;Lee, Hye Jin;Ko, Jung Min;Kang, Hee Gyung;Cheong, Hae Il;Yu, Hyeong Gon;Kim, Jae Hyung
    • Journal of Genetic Medicine
    • /
    • v.11 no.1
    • /
    • pp.31-35
    • /
    • 2014
  • Bardet-Biedl syndrome (BBS) is a rare ciliopathy generally inherited with an autosomal recessive pattern. BBS is characterized by 6 primary features namely retinal dystrophy, obesity, postaxial polydactyly, renal dysfunction, learning difficulties, and hypogonadism and a wide range of secondary features. To date, mutations in 16 genes have been identified as causative factors for BBS. Among them, the BBS1 and BBS10 genes are major disease-causing genes, and each of these gene mutations presents in more than 20% of all BBS patients. Genotype-phenotype correlations have not been observed in BBS, and there can be phenotypic overlap between BBS and other ciliopathies. In Korea, no molecular, genetically confirmed case of BBS has been reported to date. Herein, we describe the case of the first Korean siblings with BBS resulting from 2 BBS10 gene mutations who showed typical clinical phenotypes, including retinal dystrophy, obesity, intellectual disability, cystic tubular disease, and postaxial polydactyly.

Wavelength Integration Transmission Method for Hybrid-PON (Hybrid-PON을 위한 파장통합 전송방식)

  • Kim, Jin-Hee;Cheong, Ki-Tae;Chung, Hae
    • The Journal of Korean Institute of Communications and Information Sciences
    • /
    • v.34 no.11B
    • /
    • pp.1207-1215
    • /
    • 2009
  • The FTTH is known as an optimal solution to provide broadband services like IPTV and the W-PON is a good alternative to implement the FTTH. It is firstly commercialized in Korea but not widely deployed because of it's high price. In this paper, we suggest a wavelength integration method to drop the price and enhance the utilization of the W-PON. The method makes one logical channel with multiple wavelengths when the W-PON system has to accommodate a signal of which transmission rate is greater than the rate of a single wavelength. Accordingly, the system can accommodate any signal rate. We introduce a frame structure, suggest synchronization and clock recovery methods, and finally show actual applications for the Ethernet and the G-PON.

A Pediatric Case of Inflammatory Bowel Disease with Renal Amyloidosis

  • Hyun, Hyesun;Park, Eujin;Kim, Ji Hyun;Cho, Myung Hyun;Kang, Hee Gyung;Moon, Jin Soo;Moon, Kyung Chul;Ha, Il-Soo;Cheong, Hae Il
    • Childhood Kidney Diseases
    • /
    • v.22 no.2
    • /
    • pp.81-85
    • /
    • 2018
  • Amyloidosis is a rare disease that results from the deposition of extracellular protein in various body tissues, causing progressive organ dysfunction. Secondary renal amyloidosis is a rare but serious complication of chronic inflammatory bowel disease, particularly in patients with Crohn's disease or ulcerative colitis. We report a case of secondary renal amyloidosis in a pediatric patient who reported a 16-year history of "very early onset inflammatory bowel disease". Intensive treatment including repeated infliximab infusions improved clinical parameters of inflammatory bowel disease, although renal dysfunction showed progression. Amyloidosis should be considered in patients with IBD, particularly if they suffered disease progression.

산소 유량에 따라 증착된 ITO (Indium Tin Oxide)의 전기적 특성 분석

  • Kim, Dong-Hae;Son, Chan-Hui;Yun, Myeong-Su;Lee, Gyeong-Ae;Jo, Tae-Hun;Jo, Lee-Hyeon;No, Jun-Hyeong;Yu, Jin-Hyeok;Choe, Eun-Ha;Jo, Gwang-Seop;Eom, Hwan-Seop;Jeon, Bu-Il;Gwon, Gi-Cheong
    • Proceedings of the Korean Vacuum Society Conference
    • /
    • 2012.02a
    • /
    • pp.410-410
    • /
    • 2012
  • 투명 전도성 TCO (Transparent Conductivity Oxide)박막 중 ITO (Indium Tin Oxide) 박막은 n-type의 전도특성을 갖는 산화물로서 가시광선 영역에서의 높은 투과율, 전기 전도도, 넓은 밴드갭을 나타내기 때문에 디스플레이 및 태양전지 분야에 널리 사용 되어 지고 있다. 이 실험에서는 ITO 증착시 산소 유량의 변화에 따라 특성의 변화를 관찰하고자 실험을 진행 하였다. 실험에서 산소 유량은 0 sccm에서 12 sccm까지 변화를 주었으며, ITO는 RF 마그네트론 스퍼터를 이용하여 유리위에 증착하였다. 실험에서 인가된 RF power는 2 kW, 13.56 MHz, 공정 압력은 $4.5{\times}10^{-6}torr$에서 진행하였다. 유리와 타겟 사이의 거리는 200 mm로 고정하였으며, 온도는 상온에서 공정을 진행하였다. 증착된 ITO의 전기전도도(${\sigma}$)는 3 sccm까지는 증가하는 경향을 보이다가 그 이후부터는 감소하는 것을 확인 할 수 있었다. 투과율과 이차전자방출계수의 결과 또한 전기전도도와 유사한 경향성을 보여 주었다. 이를 통해 3 sccm의 산소 유량으로 증착된 ITO의 전기적 특성이 가장 좋은 것으로 확인이 되었다.

  • PDF

WOLSONG LOW- AND INTERMEDIATE-LEVEL RADIOACTIVE WASTE DISPOSAL CENTER: PROGRESS AND CHALLENGES

  • Park, Jin-Beak;Jung, Hae-Ryong;Lee, Eun-Young;Kim, Chang-Lak;Kim, Geon-Young;Kim, Kyung-Su;Koh, Yong-Kwon;Park, Kyung-Woo;Cheong, Jae-Hak;Jeong, Chan-Woo;Choi, Jong-Soo;Kim, Kyung-Deok
    • Nuclear Engineering and Technology
    • /
    • v.41 no.4
    • /
    • pp.477-492
    • /
    • 2009
  • In this paper, we discuss the experiences during the preparation of the Wolsong Low- and Intermediate-Level Radioactive Waste Disposal Center. These experiences have importance as a first implementation for the national LILW disposal facility in the Republic of Korea. As for the progress, it relates to the area of selected disposal site, the disposal site characteristics, waste characteristics of the disposal facility, safety assessment, and licensing process. During these experiences, we also discuss the necessity for new organization and change for a radioactive waste management system. Further effort for the safe management of radioactive waste needs to be pursued.

Electrical Breakdown Characteristics of Epoxy and dry-air Composite Insulation (에폭시와 dry-air 혼합절연물의 절연파괴특성)

  • Jung, Hae-Eun;Oh, Jin-Heon;Lim, Jong-Nam;Kang, Seong-Hwa;Lim, Kee-Jo
    • Proceedings of the KIEE Conference
    • /
    • 2007.07a
    • /
    • pp.1389-1390
    • /
    • 2007
  • SF6 gas used widely as insulating component is rising as the environment problem. Electrical breakdown characteristics of epoxy and dry-air composite insulation was investigated on thickness of epoxy and pressure of dry-air under non-uniform field. The gap of needle to plane was from 2mm to 5mm. The pressure of dry-air was varied within the range of $0.1{\sim}0.6$ MPa. The thickness of a needle was 1mm and the curvature radius of a needle end was 100um. The diameter of a plane made of the stainless steel was 50mm. As a result of the experiment, breakdown voltage was increased about 3 times when epoxy was used. The impact that the thickness of epoxy influences on breakdown voltage was poor. It needs suitable thickness computation because the insulating gap of the gas is short as epoxy thickness increases.

  • PDF

A Case of Membranoproliferative Glomerulonephritis Superimposed on Type 1 Diabetes Mellitus (제1형 당뇨병 환자에서 병발한 막증식성 사구체신염 1례)

  • Choi Hyun-Jin;Cho, Hee-Yeon;Kang Ju-Hyeong;Yang Sei-Won;Cheong Hae-Il;Choi Yong;Moon Kyung-Chul;Ha Il-Soo
    • Childhood Kidney Diseases
    • /
    • v.9 no.1
    • /
    • pp.97-101
    • /
    • 2005
  • Renal diseases other than diabetic nephropathy can occur In diabetic patients. Urinary abnormalities or clinical courses inconsistent with the natural progression of diabetic nephropathy are suggestive of non-diabetic renal diseases and should lead to more extensive investigations. Presence of non-diabetic renal diseases in diabetic patients can alter the treatment plan and the prognosis. We report a 9-year-old girl who had type 1 membranoproliferatiye glomerulonephritis as well as type 1 diabetes mellitus.

  • PDF

Genotoxicity of Heavy Metals among the Particulates in the Working Environment as Assessed by Tradescantia-Micronucleus (Trad-MCN) Assay (자주달개비 미세핵 분석법을 이용한 작업환경내 총 먼지 중 수용성 추출물의 유전독성 평가)

  • Shin, Hae-Shik;Kim, Jin-Kyu;Lee, Jae-Hwan;Hwang, Kap-Sung;Kim, Kyun;Lee, Jeong-Joo;Lee, Jin-Hong
    • Journal of Korean Society for Atmospheric Environment
    • /
    • v.19 no.6
    • /
    • pp.639-646
    • /
    • 2003
  • In this study, we evaluated genotoxicity of heavy metals among particulates with Tradescantia-micronucleus (Trad-MCN) assay in the various working environment. In a synthetic fiber factory and a rubber factory, chromium concentration was higher than any other heavy metals. On the other hand, nickel concentration was the highest in a semi-conductor factory. The difference in genotoxicity among the working environment was statistically significant as Trad-MCN frequencies were 4.07 $\pm$0.35 MCN/100 tetrads (p< 0.01) for the synthetic fiber factory,5.73 $\pm$0.81 MCN/100 tetrads (p< 0.01) for the rubber factory, and 15.60$\pm$2.58 (p< 0.01) (p< 0.001) for the semi -conductor factory. As a result, heavy metals among particulates in the working environment can be considered to have hazardous potential to human health, although they cannot directly induce DNA damage to the workers in the working environments.

Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome

  • Chang, Hye Jin;Kim, Hwa Young;Choi, Jae Hong;Choi, Hyun Jin;Ko, Jae Sung;Ha, Il Soo;Cheong, Hae Il;Choi, Yong;Kang, Hee Gyung
    • Clinical and Experimental Pediatrics
    • /
    • v.57 no.2
    • /
    • pp.96-99
    • /
    • 2014
  • Hemolytic uremic syndrome (HUS) is one of the most common causes of acute renal failure in childhood and is primarily diagnosed in up to 4.5% of children who undergo chronic renal replacement therapy. Escherichia coli serotype O157:H7 is the predominant bacterial strain identified in patients with HUS; more than 100 types of Shiga toxin-producing enterohemorrhagic E. coli (EHEC) subtypes have also been isolated. The typical HUS manifestations are microangiopathic hemolytic anemia, thrombocytopenia, and renal insufficiency. In typical HUS cases, more serious EHEC manifestations include severe hemorrhagic colitis, bowel necrosis and perforation, rectal prolapse, peritonitis, and intussusceptions. Colonic perforation, which has an incidence of 1%-2%, can be a fatal complication. In this study, we report a typical Shiga toxin-associated HUS case complicated by small intestinal perforation with refractory peritonitis that was possibly because of ischemic enteritis. Although the degree of renal damage is the main concern in HUS, extrarenal complications should also be considered in severe cases, as presented in our case.