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常染色体显性纯合遗传性痉挛性截瘫(SPG19)的新基因座定位于9号染色体q33 - q34区域。

Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34.

作者信息

Valente Enza Maria, Brancati Francesco, Caputo Viviana, Bertini Enrico, Patrono Clarice, Costanti Danilo, Dallapiccola Bruno

机构信息

Neurogenetics, C.S.S. Mendel Institute, Viale Regina Margherita 261, I-00168 Rome, Italy.

出版信息

Ann Neurol. 2002 Jun;51(6):681-5. doi: 10.1002/ana.10204.

Abstract

Hereditary spastic paraplegia is a clinically and genetically heterogeneous disorder characterized by progressive spasticity of the lower limbs. Seven loci for autosomal dominant pure hereditary spastic paraplegia (ADPHSP) have already been mapped on chromosomes 14q, 2p, 15q, 8p, 12q, 19q, and 2q. We report on an Italian family affected by ADPHSP for which we excluded linkage with the known loci and performed a genome-wide search. Linkage analysis and haplotype construction permitted the identification of a novel ADPHSP locus on the long arm of chromosome 9, designated SPG19. The phenotype was characterized by late onset (range, 36-55 years) and mild disability, with only 1 patient bound to a wheelchair after 31 years of disease. Urinary disturbances (urgency and/or incontinence) were always present, even in young patients with a short disease history.

摘要

遗传性痉挛性截瘫是一种临床和遗传异质性疾病,其特征为下肢进行性痉挛。常染色体显性纯合遗传性痉挛性截瘫(ADPHSP)的7个基因座已被定位在14号染色体长臂、2号染色体、15号染色体长臂、8号染色体短臂、12号染色体长臂、19号染色体长臂和2号染色体上。我们报告了一个受ADPHSP影响的意大利家族,我们排除了该家族与已知基因座的连锁关系,并进行了全基因组搜索。连锁分析和单倍型构建使得在9号染色体长臂上鉴定出一个新的ADPHSP基因座,命名为SPG19。该疾病的表型特征为发病较晚(范围为36至55岁)且残疾程度较轻,疾病31年后仅有1例患者需要轮椅辅助。即使是病程较短的年轻患者也总是存在泌尿功能障碍(尿急和/或尿失禁)。

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