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Two forms of biotin-responsive multiple carboxylase deficiency.

作者信息

Sweetman L

出版信息

J Inherit Metab Dis. 1981;4(2):53-4. doi: 10.1007/BF02263587.

DOI:10.1007/BF02263587
PMID:6790844
Abstract

Biotin-responsive multiple carboxylase deficiencies are classified into early and late forms. The early form showed higher urinary excretion of 3-hydroxyisovalerate and 3-hydroxypropionate than the late form and was associated with normal plasma biotin concentrations. It is proposed that holocarboxylase synthetase and intestinal biotin absorption are defective in the early and late forms respectively.

摘要

相似文献

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本文引用的文献

1
A new assay method for biotin in blood, serum, urine, and tissues.一种用于检测血液、血清、尿液和组织中生物素的新检测方法。
Anal Biochem. 1962 Jan;3:31-9. doi: 10.1016/0003-2697(62)90041-6.
2
Biotin-responsive beta-methylcrotonylglycinuria.生物素反应性β-甲基巴豆酰甘氨酸尿症
Lancet. 1971 Jul 3;2(7714):22-4. doi: 10.1016/s0140-6736(71)90009-2.
3
Beta-methylcrotonic aciduria associated with lactic acidosis.与乳酸性酸中毒相关的β-甲基巴豆酸尿症。
土耳其新生儿筛查项目的发展与组织。
J Clin Lab Anal. 2014 Jan;28(1):63-9. doi: 10.1002/jcla.21645. Epub 2013 Dec 27.
4
Neurological deficits in mice with profound biotinidase deficiency are associated with demylination and axonal degeneration.严重生物素酶缺乏症小鼠的神经功能缺损与脱髓鞘和轴突变性有关。
Neurobiol Dis. 2012 Sep;47(3):428-35. doi: 10.1016/j.nbd.2012.04.016. Epub 2012 May 8.
5
Pyruvate carboxylase deficiency.丙酮酸羧化酶缺乏症
J Inherit Metab Dis. 1984;7 Suppl 1:74-8. doi: 10.1007/BF03047379.
6
The biotin-dependent carboxylase deficiencies.生物素依赖性羧化酶缺乏症
Am J Hum Genet. 1982 Sep;34(5):699-716.
7
Biotinidase deficiency: a novel vitamin recycling defect.生物素酶缺乏症:一种新型的维生素循环缺陷。
J Inherit Metab Dis. 1985;8 Suppl 1:53-8. doi: 10.1007/BF01800660.
8
Intestinal absorption and renal excretion of biotin in patients with biotinidase deficiency.生物素酶缺乏症患者生物素的肠道吸收与肾脏排泄
Eur J Pediatr. 1985 May;144(1):21-6. doi: 10.1007/BF00491919.
9
Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency.生物素反应性多种羧化酶缺乏症患者中全羧化酶合成酶的异质性
Am J Hum Genet. 1985 Mar;37(2):326-37.
10
Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities.一名血清生物素酶和成纤维细胞全羧化酶合成酶活性正常的8岁男孩患生物素反应性多种羧化酶缺乏症。
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J Pediatr. 1976 Feb;88(2):229-35. doi: 10.1016/s0022-3476(76)80987-0.
4
Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria.一名患有甲基巴豆酰甘氨酸尿症患者体内丙酰辅酶A羧化酶和甲基巴豆酰辅酶A羧化酶缺乏。
Clin Chim Acta. 1977 May 2;76(3):321-8. doi: 10.1016/0009-8981(77)90158-9.
5
Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency.一名丙酰辅酶A羧化酶缺乏症患者异亮氨酸的异常代谢产物
Biomed Mass Spectrom. 1978 Mar;5(3):198-207. doi: 10.1002/bms.1200050307.
6
Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts.生物素反应性有机酸尿症。多种羧化酶缺陷及在培养成纤维细胞中与丙酸血症的互补研究。
J Clin Invest. 1979 Dec;64(6):1695-702. doi: 10.1172/JCI109632.
7
Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity.多种生物素依赖性羧化酶缺乏症与T细胞和B细胞免疫缺陷相关。
Lancet. 1979 Jul 21;2(8134):115-8. doi: 10.1016/s0140-6736(79)90002-3.