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Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsions.

作者信息

Slot H M, Overweg-Plandsoen W C, Bakker H D, Abeling N G, Tamminga P, Barth P G, Van Gennip A H

机构信息

Academic Medical Center, Department of Neonatology, Amsterdam, The Netherlands.

出版信息

Neuropediatrics. 1993 Jun;24(3):139-42. doi: 10.1055/s-2008-1071531.

DOI:10.1055/s-2008-1071531
PMID:8355818
Abstract

Intractable seizures in the neonatal period may be caused by molybdenum-cofactor deficiency, an inborn error which combines the deficiencies of sulphite oxidase and xanthine dehydrogenase. The neurological symptoms of molybdenum cofactor and isolated sulphite oxidase deficiencies are identical. Two new cases are reported, and the literature on neonatal convulsions due to molybdenum-cofactor and sulphite deficiencies is reviewed. Because of the high incidence of neonatal convulsions a search for this deficiency is advocated in each case of unexplained refractory neonatal convulsions. Diagnosis may be missed or delayed on standard metabolic screening for several reasons discussed. By simply using a sulphite strip test in a fresh urine sample an indication for the defect can be obtained. Antenatal diagnosis can be performed by assay of sulphite oxidase activity in a chorionic villus sample.

摘要

相似文献

1
Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsions.
Neuropediatrics. 1993 Jun;24(3):139-42. doi: 10.1055/s-2008-1071531.
2
Prenatal diagnosis of molybdenum cofactor deficiency by assay of sulphite oxidase activity in chorionic villus samples.
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Isolated sulphite oxidase deficiency mimics the features of hypoxic ischaemic encephalopathy.
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The detection of molybdenum cofactor deficiency: clinical symptomatology and urinary metabolite profile.钼辅因子缺乏症的检测:临床症状学和尿代谢产物谱
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A re-evaluation of the tissue distribution and physiology of xanthine oxidoreductase.黄嘌呤氧化还原酶的组织分布与生理学的重新评估。
Histochem J. 1994 Dec;26(12):889-915.