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      KCI등재 SCI SCIE SCOPUS

      An Unusual Presentation of Diabetic Ketoacidosis in Familial Hajdu-Cheney Syndrome: A Case Report

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      https://www.riss.kr/link?id=A104796166

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      다국어 초록 (Multilingual Abstract)

      A 21-year-old man with diabetic ketoacidosis (DKA) displayed short and clubbed fingers and marked eyebrow, which are typical of Hajdu-Cheney Syndrome (HCS). Laboratory findings confirmed type 1 diabetes mellitus (DM). After conservative care with hydr...

      A 21-year-old man with diabetic ketoacidosis (DKA) displayed short and clubbed fingers and marked eyebrow, which are typical of Hajdu-Cheney Syndrome (HCS). Laboratory findings confirmed type 1 diabetes mellitus (DM). After conservative care with hydration and insulin supply, metabolic impairment was improved. Examinations of bone and metabolism revealed osteoporosis and craniofacial abnormalities. The mutation (c.6443T>G) of the NOTCH2 gene was found. The patient was diagnosed with HCS and DM. There may be a relationship between HCS and DM, with development of pancreatic symptoms related to the NOTCH2 gene mutation.

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      참고문헌 (Reference)

      1 한은진, "하쥬-체니 증후군 1예" 대한내분비학회 25 (25): 152-156, 2010

      2 Stathopoulos IP, "Severe osteoporosis and mutation in NOTCH2 gene in a woman with Hajdu-Cheney syndrome" 52 : 366-371, 2013

      3 Bar Y, "Redifferentiation of expanded human pancreatic β-cell-derived cells by inhibition of the NOTCH pathway" 287 : 17269-17280, 2012

      4 Ornetti P, "Osteoporotic compression fracture revealing Hajdu-Cheney syndrome" 79 : 514-515, 2012

      5 Afelik S, "Notch-mediated patterning and cell fate allocation of pancreatic progenitor cells" 139 : 1744-1753, 2012

      6 Li HJ, "Notch signaling differentially regulates the cell fate of early endocrine precursor cells and their maturing descendants in the mouse pancreas and intestine" 371 : 156-169, 2012

      7 Zanotti S, "Notch regulation of bone development and remodeling and related skeletal disorders" 90 : 69-75, 2012

      8 Lammert E, "Notch gene expression during pancreatic organogenesis" 94 : 199-203, 2000

      9 McDaniell R, "NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway" 79 : 169-173, 2006

      10 Majewski J, "Mutations in NOTCH2 in families with Hajdu-Cheney syndrome" 32 : 1114-1117, 2011

      1 한은진, "하쥬-체니 증후군 1예" 대한내분비학회 25 (25): 152-156, 2010

      2 Stathopoulos IP, "Severe osteoporosis and mutation in NOTCH2 gene in a woman with Hajdu-Cheney syndrome" 52 : 366-371, 2013

      3 Bar Y, "Redifferentiation of expanded human pancreatic β-cell-derived cells by inhibition of the NOTCH pathway" 287 : 17269-17280, 2012

      4 Ornetti P, "Osteoporotic compression fracture revealing Hajdu-Cheney syndrome" 79 : 514-515, 2012

      5 Afelik S, "Notch-mediated patterning and cell fate allocation of pancreatic progenitor cells" 139 : 1744-1753, 2012

      6 Li HJ, "Notch signaling differentially regulates the cell fate of early endocrine precursor cells and their maturing descendants in the mouse pancreas and intestine" 371 : 156-169, 2012

      7 Zanotti S, "Notch regulation of bone development and remodeling and related skeletal disorders" 90 : 69-75, 2012

      8 Lammert E, "Notch gene expression during pancreatic organogenesis" 94 : 199-203, 2000

      9 McDaniell R, "NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway" 79 : 169-173, 2006

      10 Majewski J, "Mutations in NOTCH2 in families with Hajdu-Cheney syndrome" 32 : 1114-1117, 2011

      11 Simpson MA, "Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss" 43 : 303-305, 2011

      12 Currarino G, "Hajdu-Cheney syndrome associated with serpentine fibulae and polycystic kidney disease" 39 : 47-52, 2009

      13 Brennan AM, "Hajdu-Cheney syndrome : evolution of phenotype and clinical problems" 100 : 292-310, 2001

      14 Ninov N, "Different levels of Notch signaling regulate quiescence, renewal and differentiation in pancreatic endocrine progenitors" 139 : 1557-1567, 2012

      15 Hajdu N, "Cranio-skeletal dysplasia" 21 : 42-48, 1948

      16 Narumi Y, "Clinical consequences in truncating mutations in exon 34 of NOTCH2: report of six patients with Hajdu-Cheney syndrome and a patient with serpentine fibula polycystic kidney syndrome" 161 : 518-526, 2013

      17 Kung AW, "Association of JAG1 with bone mineral density and osteoporotic fractures : a genome-wide association study and follow-up replication studies" 86 : 229-239, 2010

      18 Cheney WD, "Acro-osteolysis" 94 : 595-607, 1965

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 SCI 등재 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.48 0.37 1.06
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.85 0.75 0.691 0.11
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