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Niemann-Pick variant lipidosis presenting as "neonatal hepatitis".

作者信息

Semeraro L A, Riely C A, Kolodny E H, Dickerson G R, Gryboski J D

出版信息

J Pediatr Gastroenterol Nutr. 1986 May-Jun;5(3):492-500. doi: 10.1097/00005176-198605000-00030.

DOI:10.1097/00005176-198605000-00030
PMID:3723274
Abstract

Neonatal hepatitis is a nonspecific term that may include a variety of disease entities. Two patients are presented who developed jaundice in the neonatal period and progressive hepatosplenomegaly. The infants were initially felt to have "neonatal hepatitis" but were subsequently found to have Niemann-Pick disease. Biochemical investigation revealed normal levels of sphingomyelinase activity in leukocytes and liver but diminished levels in cultured skin fibroblasts, compatible with Niemann-Pick type C.

摘要

相似文献

1
Niemann-Pick variant lipidosis presenting as "neonatal hepatitis".
J Pediatr Gastroenterol Nutr. 1986 May-Jun;5(3):492-500. doi: 10.1097/00005176-198605000-00030.
2
Niemann-pick disease type C in neonatal cholestasis at a North American Center.北美某中心新生儿胆汁淤积症中的C型尼曼-匹克病
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Niemann-Pick disease type C presenting as neonatal hepatitis: report of one case.表现为新生儿肝炎的C型尼曼-匹克病:一例报告
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Hepatosplenomegaly and progressive neurological symptoms - Late manifestation of Niemann-Pick disease type C - a case report -.肝脾肿大与进行性神经症状——尼曼-匹克病C型的晚期表现——病例报告
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Gaucher and Niemann-Pick diseases--enzymatic diagnosis in dried blood spots on filter paper: retrospective diagnoses in newborn-screening cards.戈谢病和尼曼-匹克病——滤纸干血斑中的酶学诊断:新生儿筛查卡片中的回顾性诊断
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Studies on the activation of sphingomyelinase activity in Niemann-Pick type A, B, and C fibroblasts: enzymological differentiation of types A and B.关于尼曼-匹克病A型、B型和C型成纤维细胞中鞘磷脂酶活性激活的研究:A型和B型的酶学鉴别
Pediatr Res. 1984 Nov;18(11):1088-93. doi: 10.1203/00006450-198411000-00006.
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[Activators for sphingohydrolases and the nature of the sphingomyelinase deficiency in Niemann-Pick disease types A, B and C (author's transl)].[鞘氨醇水解酶激活剂与A、B、C型尼曼-匹克病中鞘磷脂酶缺乏的本质(作者译)]
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[Early infantile form of Niemann-Pick disease type C. Apropos of 2 siblings].[尼曼-匹克病C型早发型婴儿型。关于2名兄弟姐妹]
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Niemann-Pick type C disease.尼曼-匹克C型病
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Sphingomyelinase activities of various human tissues in control subjects and in Niemann-Pick disease - development and evaluation of a microprocedure.对照受试者及尼曼-匹克病患者各种人体组织的鞘磷脂酶活性——一种微量方法的建立与评估
Clin Chim Acta. 1980 Oct 9;106(3):257-67. doi: 10.1016/0009-8981(80)90309-5.

引用本文的文献

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Lysosomal storage disorders in the newborn.新生儿溶酶体贮积症
Pediatrics. 2009 Apr;123(4):1191-207. doi: 10.1542/peds.2008-0635.
2
Fetal Niemann-Pick disease type C: ultrastructural and lipid findings in liver and spleen.胎儿型尼曼-匹克病C型:肝脏和脾脏的超微结构及脂质研究结果
Virchows Arch A Pathol Anat Histopathol. 1993;422(3):253-9. doi: 10.1007/BF01621810.
3
Niemann-Pick-like liver disease and reduced cholesterol esterification in fibroblasts of two male infants.两名男婴的尼曼-匹克样肝病及成纤维细胞中胆固醇酯化减少
Eur J Pediatr. 1994 May;153(5):347-51. doi: 10.1007/BF01956417.