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与转钴胺素II基因多态性776C→G相关的类固醇反应性功能性维生素B12缺乏症

Steroid-responsive functional B12 deficiency in association with transcobalamin II polymorphism 776C --> G.

作者信息

Gale Daniel P, Cobbold Jeremy F, Chataway Jeremy

机构信息

Department of Neurology, St Mary's Hospital, London, UK.

出版信息

Eur J Haematol. 2006 Jan;76(1):75-8. doi: 10.1111/j.1600-0609.2005.00563.x.

Abstract

We present a case of intracellular vitamin B12 deficiency presenting with confusion, subacute combined degeneration of the cord, megaloblastic anaemia and intrinsic factor antibodies in the serum. Diagnosis was delayed by a normal serum B12 level and was confirmed by a grossly elevated serum homocysteine. There was a dramatic response to steroids. The patient was heterozygous for the transcobalamin (TC) II polymorphism 776C --> G. This case demonstrates the importance of functional assessment of intracellular B12 activity (e.g. serum homocysteine) in excluding B12 deficiency, the role of steroids in pernicious anaemia and a possible clinical correlation of a TCII polymorphism.

摘要

我们报告一例细胞内维生素B12缺乏病例,该患者表现为意识模糊、脊髓亚急性联合变性、巨幼细胞贫血以及血清中存在内因子抗体。血清维生素B12水平正常导致诊断延迟,而血清同型半胱氨酸显著升高则证实了诊断。患者对类固醇治疗反应显著。该患者转钴胺素(TC)II基因多态性776C→G为杂合子。本病例表明细胞内B12活性功能评估(如血清同型半胱氨酸)在排除B12缺乏方面的重要性、类固醇在恶性贫血中的作用以及TCII基因多态性可能存在的临床关联。

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