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Genetic analysis of phytosterolaemia.

作者信息

Togo M, Toda T, Nguyen L A, Kubota S, Tsukamoto K, Satoh H, Hara M, Iso-o N, Noto H, Kimura S, Nakahara K, Seyama Y, Hashimoto Y

机构信息

Department of Internal Medicine, Graduate School of Medicine, The University of Tokyo, Japan.

出版信息

J Inherit Metab Dis. 2001 Feb;24(1):43-50. doi: 10.1023/a:1005650605042.

DOI:10.1023/a:1005650605042
PMID:11286381
Abstract

Two women with multiple xanthomas, intermittent arthritis and thrombocytopenia were diagnosed as phytosterolaemia, an autosomal-recessive lipid storage disease, based on their increased serum concentrations of beta-sitosterol, campesterol and sitostanol. The gene responsible for this disease is located within a distance of 18 cM between microsatellite markers of D2S 1788 and D2S1352 at chromosome 2p21. We genotyped the patients and their family members with 16 microsatellite markers around this locus. The results from the homozygosity mapping of one family suggested that the gene was located within the distance of 12.6 cM between D2S2328 and D2S1352. We have shortened the genetic distance by 5.4 cM.

摘要

相似文献

1
Genetic analysis of phytosterolaemia.
J Inherit Metab Dis. 2001 Feb;24(1):43-50. doi: 10.1023/a:1005650605042.
2
Phytosterolaemia: diagnosis, characterization and therapeutical approaches.植物甾醇血症:诊断、特征及治疗方法
Ann Med. 1997 Jun;29(3):181-4. doi: 10.3109/07853899708999333.
3
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Eur J Hum Genet. 2001 May;9(5):375-84. doi: 10.1038/sj.ejhg.5200628.
5
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemia.通过下一代测序技术对两名重度高胆固醇血症儿童进行谷甾醇血症的及时诊断。
Atherosclerosis. 2017 Jul;262:71-77. doi: 10.1016/j.atherosclerosis.2017.05.002. Epub 2017 May 4.
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Phytosterolaemia in a Norwegian family: diagnosis and characterization of the first Scandinavian case.一个挪威家庭中的植物甾醇血症:首例斯堪的纳维亚病例的诊断与特征分析
Scand J Clin Lab Invest. 1996 May;56(3):229-40. doi: 10.3109/00365519609088612.
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Identification of beta-sitosterol, campesterol, and stigmasterol in human serum.
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Specific macrothrombocytopenia/hemolytic anemia associated with sitosterolemia.特发性巨血小板减少症/溶血性贫血与植物固醇血症相关。
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High-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus.包含谷甾醇血症基因座的人类染色体2p21的高分辨率物理图谱和转录图谱。
Eur J Hum Genet. 2001 May;9(5):364-74. doi: 10.1038/sj.ejhg.5200627.
10
[Clinical and gene study of three pedigrees of phytosterolemia associated with macrothrombocytopenia and hemolysis].[三例伴有巨大血小板减少症和溶血的植物甾醇血症家系的临床及基因研究]
Zhonghua Xue Ye Xue Za Zhi. 2011 May;32(5):331-6.

本文引用的文献

1
Inhibition of cholesterol absorption by plant sterols for mass intervention.
Curr Opin Lipidol. 1998 Dec;9(6):527-31. doi: 10.1097/00041433-199812000-00003.
2
Mapping a gene involved in regulating dietary cholesterol absorption. The sitosterolemia locus is found at chromosome 2p21.定位一个参与调节膳食胆固醇吸收的基因。植物甾醇血症基因座位于2号染色体的2p21区域。
J Clin Invest. 1998 Sep 1;102(5):1041-4. doi: 10.1172/JCI3963.
3
Sitosterolemia: exclusion of genes involved in reduced cholesterol biosynthesis.谷甾醇血症:排除参与胆固醇生物合成减少的基因。
J Lipid Res. 1998 May;39(5):1055-61.
4
Competitive inhibition of hepatic sterol 27-hydroxylase by sitosterol: decreased activity in sitosterolemia.植物甾醇对肝脏胆固醇27-羟化酶的竞争性抑制作用:在植物甾醇血症中活性降低。
Proc Assoc Am Physicians. 1998 Jan-Feb;110(1):32-9.
5
The organization of the human gene NCX1 encoding the sodium-calcium exchanger.编码钠钙交换体的人类基因NCX1的结构
Genomics. 1996 Oct 1;37(1):105-12. doi: 10.1006/geno.1996.0526.
6
Isolation and characterization of the human cytochrome P450 CYP1B1 gene.人细胞色素P450 CYP1B1基因的分离与鉴定
J Biol Chem. 1996 Nov 8;271(45):28324-30. doi: 10.1074/jbc.271.45.28324.
7
Genetic linkage mapping of the human steroid 5 alpha-reductase type 2 gene (SRD5A2) close to D2S352 on chromosome region 2p23-->p22.人2型类固醇5α-还原酶基因(SRD5A2)的遗传连锁图谱定位于染色体2p23→p22区域,靠近D2S352。
Cytogenet Cell Genet. 1996;73(4):304-7. doi: 10.1159/000134362.
8
The chromosomal localization of the human follicle-stimulating hormone receptor gene (FSHR) on 2p21-p16 is similar to that of the luteinizing hormone receptor gene.
Genomics. 1993 Jan;15(1):222-4. doi: 10.1006/geno.1993.1041.
9
Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin.人β-血影蛋白(β-肌动蛋白的非红细胞形式)染色体基因和cDNA部分的克隆。
Genomics. 1993 Aug;17(2):287-93. doi: 10.1006/geno.1993.1323.
10
Biochemical studies of inherited diseases related to abnormal cholesterol metabolism. II: Absence of unusual C28 and C29 bile acid homologs in bile and urine of sitosterolemia.与异常胆固醇代谢相关的遗传性疾病的生化研究。II:谷甾醇血症患者胆汁和尿液中异常C28和C29胆汁酸同系物的缺失
Hiroshima J Med Sci. 1994 Sep;43(3):81-6.