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对患有显性视网膜色素变性的家族进行的视网膜电图研究。

Electroretinographic studies of families with dominant retinitis pigmentosa.

作者信息

Andréasson S

机构信息

Department of Ophthalmology, University Hospital of Lund, Sweden.

出版信息

Acta Ophthalmol (Copenh). 1991 Apr;69(2):162-8. doi: 10.1111/j.1755-3768.1991.tb02706.x.

Abstract

Full-field electroretinograms were recorded from four different families with dominant retinitis pigmentosa. Two different types of the disease were recognizable and consistent within each pedigree, one with normal cone b-wave implicit times (one pedigree) and the other with prolonged cone b-wave implicit times (three pedigrees). The cone b-wave amplitude was found to decrease with age, but the implicit time did not, suggesting that the amplitude is useful for monitoring the progression of the disease whereas the implicit time seems more suitable for distinguishing different types of the disease. The progression rate was analyzed in a large pedigree, spanning six generations, three of which were examined in detail. The recently described Pro23His gene was not detected in the families.

摘要

对四个患有显性视网膜色素变性的不同家族进行了全视野视网膜电图记录。在每个家系中可识别出两种不同类型的疾病,且具有一致性,一种是视锥细胞b波潜伏时正常(一个家系),另一种是视锥细胞b波潜伏时延长(三个家系)。发现视锥细胞b波振幅随年龄降低,但潜伏时未降低,这表明振幅有助于监测疾病进展,而潜伏时似乎更适合区分不同类型的疾病。在一个跨越六代的大家系中分析了疾病进展率,其中三代进行了详细检查。这些家族中未检测到最近描述的Pro23His基因。

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