Meitinger T, Fraser N A, Lorenz B, Zrenner E, Murken J, Craig I W
Genetics Laboratory, Department of Biochemistry, University of Oxford, UK.
Hum Genet. 1989 Feb;81(3):283-6. doi: 10.1007/BF00279005.
A hypervariable DNA marker is closely linked to one of the most severe forms of night blindness, X-linked retinitis pigmentosa (RP). Affected individuals with X-linked RP, obligate carriers, and ophthalmologically identifiable carriers of the disease were included in a linkage study. The diagnosis was established in five sibships by funduscopic and electrophysiological investigations. When the X-linked probe M27 beta was used, 2 recombinants out of 29 informative meioses were detected (theta = 0.07 at a maximum lod of 4.75). The hypervariable probe detected two different alleles in 38 of 39 females tested. M27 beta is therefore a potentially very useful probe for carrier detection and prenatal diagnosis, as well as for addressing the question of heterogeneity of X-linked RP.
一种高变DNA标记与最严重的夜盲症形式之一——X连锁视网膜色素变性(RP)紧密连锁。患有X连锁RP的患者、肯定携带者以及该疾病在眼科可识别的携带者被纳入一项连锁研究。通过眼底镜检查和电生理检查在五个家系中确立了诊断。当使用X连锁探针M27β时,在29个信息减数分裂中检测到2个重组体(在最大lod值为4.75时,θ = 0.07)。在39名接受检测的女性中,高变探针在38名女性中检测到两个不同的等位基因。因此,M27β对于携带者检测和产前诊断以及解决X连锁RP的异质性问题可能是一种非常有用的探针。