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在一个大型德国家系中,具有遗传早现现象的常染色体显性遗传性痉挛性截瘫定位于2号染色体p21 - p24区域的一个4厘摩区间。

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.

作者信息

Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A

机构信息

Institute of Human Genetics, Virchow-Klinikum, Humboldt-Universität, Berlin, Germany.

出版信息

Hum Genet. 1996 Sep;98(3):371-5. doi: 10.1007/s004390050223.

Abstract

Autosomal dominant familial spastic paraplegias (AD-FSP) are a group of genetically heterogeneous diseases characterised by a progressive spasticity of the lower limbs. Three loci have already been identified by genetic linkage studies on chromosomes 2p, 14q and 15q. Here we present linkage data from a large German family displaying AD-FSP with anticipation which confirms the existence of the FSP2 locus on chromosome 2p. The recombination events observed in our family define the critical region for the FSP2 gene to be within a 4-cM interval, flanked by markers D2S400 and D2S367. Moreover, clinical data from our family show evidence of anticipation, a phenomenon caused by trinucleotide expansion in several other neurodegenerative diseases.

摘要

常染色体显性遗传性家族性痉挛性截瘫(AD - FSP)是一组具有遗传异质性的疾病,其特征为下肢进行性痉挛。通过对2号染色体、14号染色体和15号染色体的遗传连锁研究,已经确定了三个基因座。在此,我们展示了一个表现出遗传早现的德国大家系的连锁数据,该家系患有AD - FSP,这证实了2号染色体上FSP2基因座的存在。在我们的家系中观察到的重组事件确定了FSP2基因的关键区域位于一个4厘摩的区间内,两侧为标记D2S400和D2S367。此外,我们家系的临床数据显示出遗传早现的证据,这是一种由其他几种神经退行性疾病中的三核苷酸扩增引起的现象。

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