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Wolman's disease: clinical, biochemical and ultrastructural studies in an unusual case without striking adrenal calcification.

作者信息

Schaub J, Janka G E, Christomanou H, Sandhoff K, Permanetter W, Hübner G, Meister P

出版信息

Eur J Pediatr. 1980 Oct;135(1):45-53. doi: 10.1007/BF00445892.

DOI:10.1007/BF00445892
PMID:7449788
Abstract

A case of Wolman's disease is described in a German infant who died at the age of 4 months. Hepatosplenomegaly, abdominal distention, gastrointestinal symptoms, dyserythropoietic changes in the bone marrow, but not adrenal calcification on X-ray were present. Stored lipid material could be demonstrated in liver, spleen, intestine, adrenals, thymus, kidneys, blood cells, but not in the central nervous system. Cholesterylesters and triglycerides were markedly increased in liver and spleen. Lysosomal acid lipase was found to be decreased in leucocytes and liver to less than 10% of normal, when measured with synthetic and natural substrates.

摘要

相似文献

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Wolman's disease: clinical, biochemical and ultrastructural studies in an unusual case without striking adrenal calcification.
Eur J Pediatr. 1980 Oct;135(1):45-53. doi: 10.1007/BF00445892.
2
Wolman's disease. Ultrasound and CT diagnosis.沃尔曼病。超声与CT诊断。
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Characteristics of acid esterase in Wolman's disease.沃尔曼病中酸性酯酶的特征
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Lymphoid cell lines as a model system for the study of Wolman's disease: enzymatic, metabolic and ultrastructural investigations.作为研究沃尔曼病模型系统的淋巴样细胞系:酶学、代谢及超微结构研究
J Inherit Metab Dis. 1986;9(2):193-201. doi: 10.1007/BF01799458.
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[Lipid storage disease similar to Wolman's disease in humans in the fox terrier].[猎狐梗中与人类沃尔曼病相似的脂质贮积病]
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Neutral lipid storage with acid lipase deficiency: a new variant of Wolman's disease with features of the Senior syndrome.伴有酸性脂肪酶缺乏的中性脂质贮积症:一种具有西尼尔综合征特征的沃尔曼病新变体。
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[Acid lipases and acid cholesterol esterases: Wolman's disease and cholesteryl ester storage disease].[酸性脂肪酶和酸性胆固醇酯酶:沃尔曼病和胆固醇酯贮积病]
Pathol Biol (Paris). 1988 Feb;36(2):167-81.
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[Hepatic cholesterolosis. Histological, histochemical and ultrastructural study of 2 cases].[肝胆固醇沉着症。2例的组织学、组织化学及超微结构研究]
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Genetic lipid storage disease with lysosomal acid lipase deficiency in rats.大鼠中伴有溶酶体酸性脂肪酶缺乏的遗传性脂质贮积病
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本文引用的文献

1
Niemann-Pick disease; report of a case showing calcification in the adrenal glands.尼曼-匹克病;一例肾上腺钙化病例报告。
N Z Med J. 1946 Feb;45:43-5.
2
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Wolman's disease.沃尔曼病
儿童患者溶酶体酸性脂肪酶缺乏症:范围综述。
J Pediatr (Rio J). 2022 Jan-Feb;98(1):4-14. doi: 10.1016/j.jped.2021.03.003. Epub 2021 May 6.
4
Targeting Wolman Disease and Cholesteryl Ester Storage Disease: Disease Pathogenesis and Therapeutic Development.靶向沃尔曼病和胆固醇酯贮积病:疾病发病机制与治疗进展
Curr Chem Genom Transl Med. 2017 Jan 30;11:1-18. doi: 10.2174/2213988501711010001. eCollection 2017.
5
Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infants.婴儿期溶酶体酸性脂肪酶缺乏症的快速进展与死亡率
Genet Med. 2016 May;18(5):452-8. doi: 10.1038/gim.2015.108. Epub 2015 Aug 27.
6
A splice junction mutation causes deletion of a 72-base exon from the mRNA for lysosomal acid lipase in a patient with cholesteryl ester storage disease.在一名患有胆固醇酯贮积病的患者中,剪接连接突变导致溶酶体酸性脂肪酶的mRNA缺失一个72个碱基的外显子。
J Clin Invest. 1993 Dec;92(6):2713-8. doi: 10.1172/JCI116888.
7
Screening for lysosomal disorders.溶酶体疾病的筛查。
Eur J Pediatr. 1994;153(7 Suppl 1):S38-43. doi: 10.1007/BF02138776.
8
Prenatal monitoring for Wolman's disease in a pregnancy at risk: first case in the Federal Republic of Germany.对有风险的妊娠进行沃曼病的产前监测:德意志联邦共和国首例病例。
Hum Genet. 1981;57(4):440-1. doi: 10.1007/BF00281702.
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Wolman's disease. Ultrasound and CT diagnosis.沃尔曼病。超声与CT诊断。
Pediatr Radiol. 1985;15(2):144-6. doi: 10.1007/BF02388726.
10
Wolman's disease: ultrasonographic and computed tomographic findings.沃尔曼病:超声和计算机断层扫描表现
Pediatr Radiol. 1992;22(7):541-2. doi: 10.1007/BF02013008.
Arch Dis Child. 1970 Oct;45(243):710. doi: 10.1136/adc.45.243.710-b.
4
Acid lipase in cultured fibroblasts: cholesterol ester storage disease.培养成纤维细胞中的酸性脂肪酶:胆固醇酯贮积病
J Lab Clin Med. 1974 Jul;84(1):54-61.
5
Wolman disease with jaundice and subarachnoid hemorrhage.伴有黄疸和蛛网膜下腔出血的沃尔曼病
Am J Dis Child. 1973 Nov;126(5):671-5. doi: 10.1001/archpedi.1973.02110190541017.
6
Wolman's disease: report of two new cases, with a review of the literature.沃尔曼病:两例新病例报告及文献综述
Am J Clin Pathol. 1973 Apr;59(4):490-7. doi: 10.1093/ajcp/59.4.490.
7
Neonatal diagnosis of familial type-II hyperlipoproteinaemia.家族性Ⅱ型高脂蛋白血症的新生儿诊断
Lancet. 1973 Jan 20;1(7795):118-21. doi: 10.1016/s0140-6736(73)90194-3.
8
Wolman disease in a Pakistani infant.一名巴基斯坦婴儿患沃曼病。
Am J Dis Child. 1976 May;130(5):545-7. doi: 10.1001/archpedi.1976.02120060091016.
9
A simple and novel method for tritium labeling of gangliosides and other sphingolipids.
Biochim Biophys Acta. 1978 Apr 28;529(1):106-14. doi: 10.1016/0005-2760(78)90108-x.
10
Isoelectric focusing pattern of acid hydrolases in cultured fibroblasts, leucocytes and cell-free amniotic fluid.培养的成纤维细胞、白细胞和无细胞羊水酸性水解酶的等电聚焦图谱。
Neuropadiatrie. 1977 Aug;8(3):238-52. doi: 10.1055/s-0028-1091520.