Goldblatt J, Ballo R, Sachs B, Moosa A
Department of Human Genetics, University of Cape Town, South Africa.
Clin Genet. 1989 Feb;35(2):116-20. doi: 10.1111/j.1399-0004.1989.tb02915.x.
Hereditary spastic paraplegia (HSP) is rarely inherited in an X-linked recessive mode in pure and complicated forms. Recently, molecular linkage studies have suggested that these variant X-linked HSP conditions result from locus heterogeneity. In this paper we report on the clinical and linkage analysis of a kindred with complicated X-linked HSP. The finding in this family of a map location of the putative HSP gene in the same region as the documented for the pure HSP gene provides evidence that allelic mutations might also be responsible for the variable phenotype encountered in these X-linked disorders.
遗传性痉挛性截瘫(HSP)很少以单纯和复杂形式呈X连锁隐性模式遗传。最近,分子连锁研究表明,这些变异的X连锁HSP病症是由基因座异质性导致的。在本文中,我们报告了一个复杂型X连锁HSP家系的临床和连锁分析。该家族中假定的HSP基因的图谱定位与已记录的纯合HSP基因位于同一区域,这一发现提供了证据,表明等位基因突变也可能是这些X连锁疾病中出现可变表型的原因。