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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 35 Issue 10
Oct.  2019
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Diagnosis and treatment of adult Alagille syndrome:A case report

DOI: 10.3969/j.issn.1001-5256.2019.10.034
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  • Published Date: 2019-10-20
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  • [1] ALAGILLE D,ODIEVRE M,GAUTIER M,et al. Hepatic ductular hypoplasia associated with characteristic facies,vertebral malformations,retarded physical,mental,and sexual development,and cardiac murmur[J]. Pediatr,1975,86(1):63-71.
    [2] LEONARD LD,CHAO G,BAKER A,et al. Clinical utility gene card for:Alagille syndrome(ALGS)[J]. Eur J Hum Genet,2014,22(3):e1-e4.
    [3] GROCHOWSKI CM,LOOMES KM,SPINNER NB. Jagged1(JAG1):Structure,expression,and disease associations[J]. Gene,2016,576(1 Pt 3):381-384.
    [4] MA YL,SONG YZ. Advances in the diagnosis and treatment of Alagille syndrome[J]. Chin J Contemp Pediatr,2014,16(11):1188-1192.(in Chinese)马艳立,宋元宗. Alagille综合征诊断治疗进展[J].中国当代儿科杂志,2014,16(11):1188-1192.
    [5] ZHANG W,ZHAO XY,HUANG J,et al. Alagille syndrome:An uncommon cause of intrahepatic cholestasis in adults[J].Rev Esp Enferm Dig,2019,111(4):323-326.
    [6] KAMATH BM. Alagille syndrome[M]//SUCHY FJ,SOKAL RJ,BALISTRERI WF,et al. Liver disease in children. 3rd ed.New York:Cambridge University Press,2007:326-345.
    [7] GURU MURTHY GS,RANA BS,DAS A,et al. Alagille syndrome:A rare disease in an adolescent[J]. Dig Dis Sci,2012,57(11):3035-3057.
    [8] TURNPENNY PD,ELLARD S. Alagille syndrome:Pathogenesis,diagnosis and management[J]. Eur J Hum Genet,2012,20(3):251-257.
    [9] MOZER-GLASSBERG Y,HOJSAK I,ZEVIT N,et al. Pruritus responsive to naltrexone in a patient with cholestatic liver disease[J]. Isr Med Assoc J,2011,13(2):111-112.
    [10] LI H,LIU JJ,DENG M,et al. Clinical and genetic study of an infant with Alagille syndrome:Identification of a novel chromosomal interstitial deletion including JAG1 gene[J]. Chin J Contemp Pediatr,2017,19(10):1098-1103.(in Chinese)李华,刘佳佳,邓梅,等. Alagille综合征患儿1例临床和遗传学分析:一个包含JAG1基因的染色体新中间缺失的识别[J].中国当代儿科杂志,2017,19(10):1098-1103.
    [11] LI L,DONG J,WANG X,et al. JAG1 mutation spectrum and origin in Chinese children with clinical features of Alagille syndrome[J]. PLo S One,2015,10(6):e130355.
    [12] HU H,YANG YC,ZHANG H,et al. Alagille syndrome in a child combined with hepatocellular carcinoma:A case report and literature review[J]. J Clin Pediat,2017,35(4):253-255.(in Chinese)胡会,杨永臣,张泓,等. Alagille综合征合并肝细胞癌1例报告并文献复习[J].临床儿科杂志,2017,35(4):253-255.
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