Grøndahl J
Clin Genet. 1986 Jan;29(1):1-16. doi: 10.1111/j.1399-0004.1986.tb00767.x.
An attempt was made to trace all cases of tapeto-retinal degeneration in Norway. Four counties (fylker) were selected for personal examination of probands with a diagnosis of unspecified tapeto-retinal degeneration, retinitis pigmentosa, or Usher syndrome. The examinations led to the rejection of the diagnosis of tapeto-retinal degeneration in three persons, and in another four persons a diagnosis of choroidal dystrophy was made. The specific type diagnosis was adjusted in 26 additional persons. The results indicate that in Norway the diagnosis of retinitis pigmentosa may be made too frequently. Patients with Usher syndrome, choroideremia or cone-rod dystrophy are most often given the diagnosis of retinitis pigmentosa. Retinitis pigmentosa of pericentral type is in general not specified, and the diagnosis of tapeto-retinal degeneration without specified type diagnosis and retinitis pigmentosa are sometimes intermingled.
研究人员试图追踪挪威所有的毯层视网膜变性病例。选择了四个郡,对诊断为未明确类型的毯层视网膜变性、色素性视网膜炎或Usher综合征的先证者进行个人检查。检查结果显示,有三人被排除毯层视网膜变性的诊断,另外四人被诊断为脉络膜营养不良。另有26人的具体类型诊断得到了调整。结果表明,在挪威,色素性视网膜炎的诊断可能过于频繁。患有Usher综合征、无脉络膜症或锥杆营养不良的患者最常被诊断为色素性视网膜炎。中心周型色素性视网膜炎一般未被明确诊断,未明确类型诊断的毯层视网膜变性和色素性视网膜炎的诊断有时会相互混淆。