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对芬兰易患压迫性麻痹的遗传性神经病(HNPP)患者的DNA分析。

DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

作者信息

Silander K, Halonen P, Sara R, Kalimo H, Falck B, Savontaus M L

机构信息

Department of Medical Genetics, University Central Hospital of Turku, Finland.

出版信息

J Neurol Neurosurg Psychiatry. 1994 Oct;57(10):1260-2. doi: 10.1136/jnnp.57.10.1260.

Abstract

Hereditary neuropathy with liability to pressure palsies (HNPP) is a dominantly inherited disorder that presents as recurrent mononeuropathies precipitated by apparently trivial traumas. The presence of a deletion in 17p11.2 was analysed in 13 Finnish families with HNPP. The deletion was found in all patients who were neurologically and neurophysiologically confirmed to have HNPP. In the problematic cases the detection of the gene defect is the method of choice in the diagnosis of HNPP. Analysis of DNA can also be used to detect clinically unaffected family members.

摘要

遗传性压力易感性周围神经病(HNPP)是一种常染色体显性遗传性疾病,表现为反复出现的单神经病,由轻微创伤诱发。对13个芬兰HNPP家系进行了17p11.2缺失分析。在所有经神经学和神经生理学确诊为HNPP的患者中均发现了该缺失。在疑难病例中,检测基因缺陷是HNPP诊断的首选方法。DNA分析也可用于检测临床上未受影响的家庭成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cfc/485500/5c1ebbcdcab3/jnnpsyc00040-0102-a.jpg

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