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无家族发病的家族性淀粉样多神经病:通过放射免疫分析法检测变异型转甲状腺素蛋白携带者

Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.

作者信息

Tanaka M, Hirai S, Matsubara E, Okamoto K, Morimatsu M, Nakazato M

机构信息

Division of Neurology, Gunma University Hospital, Maebashi, Japan.

出版信息

J Neurol Neurosurg Psychiatry. 1988 Apr;51(4):576-8. doi: 10.1136/jnnp.51.4.576.

Abstract

A 47 year old woman with familial amyloidotic polyneuropathy (FAP) is reported, without familial occurrence of the disease. Her 81 year old mother and 53 year old sister were proved to be asymptomatic carriers for variant transthyretin (TTR) by means of the radioimmunoassay. It is suggested that unknown factor(s) may play a role in preventing or delaying the onset of the disease, producing variations in sex and family incidence. In order to establish the diagnosis of non-hereditary primary amyloidotic polyneuropathy, it must be confirmed that variant TTR is absent in the serum of relatives.

摘要

据报道,一名47岁患有家族性淀粉样多神经病(FAP)的女性,其家族中无该病的发病情况。通过放射免疫测定法证实,她81岁的母亲和53岁的姐姐是变异型甲状腺素转运蛋白(TTR)的无症状携带者。这表明未知因素可能在预防或延迟疾病发作中起作用,导致性别和家族发病率出现差异。为了确诊非遗传性原发性淀粉样多神经病,必须确认亲属血清中不存在变异型TTR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/345c/1032978/a09248e1a789/jnnpsyc00539-0105-a.jpg

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