Gourie-Devi M, Chaudhuri J R, Vasanth A, Saleem Q, Mutsuddi M, Gopinath M, Sarkar P S, Brahmachari S K
Department of Neurology, National Institute of Mental Health & Neuro Sciences (Deemed University), Bangalore.
Indian J Med Res. 1998 Apr;107:187-96.
The molecular genetic analyses (PCR and Southern hybridization) of Indian patients with myotonic dystrophy (DM) were carried out to determine the degree of repeat expansion and an attempt was made to correlate the repeat number with disease severity. A scoring system based on the salient clinical features was devised to objectively assess the disease severity. The repeat expansion was seen in 11 of 12 patients examined and showed an inverse correlation with the age of onset confirming the phenomenon of anticipation. This was further established in the two pedigrees studied, clearly demonstrating both clinical and genetic anticipation. The clinical severity score, however, did not correlate well with the repeat number. Nonetheless, such molecular genetic analyses may have immense value as a screening procedure to identify premutations as well as in prenatal diagnoses.
对印度强直性肌营养不良(DM)患者进行了分子遗传学分析(聚合酶链反应和Southern杂交),以确定重复序列扩增的程度,并尝试将重复序列数量与疾病严重程度相关联。设计了一种基于显著临床特征的评分系统,以客观评估疾病严重程度。在12例接受检查的患者中,有11例出现了重复序列扩增,并且与发病年龄呈负相关,证实了遗传早现现象。在研究的两个家系中进一步证实了这一点,清楚地显示了临床和遗传早现。然而,临床严重程度评分与重复序列数量的相关性并不好。尽管如此,这种分子遗传学分析作为一种识别前突变的筛查程序以及在产前诊断中可能具有巨大价值。