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find Keyword "视网膜色素变性" 19 results
  • Coats型视网膜色素变性一例

    报告1例女性患者,双眼非典型视网膜色素变性,右眼并Coats病样改变,经眼底荧光血管造影、ERG检查证实。右眼行激光光凝治疗。对本病的临床特点、病因、鉴别诊断、预后、治疗进行了讨论。 (中华眼底病杂志,1993,9:244-245)

    Release date:2016-09-02 06:35 Export PDF Favorites Scan
  • 203例原发性视网膜色素变性遗传类型及并发症分析

    原发性视网膜色素变性 (RP)为遗传性眼病,其遗传类型分常染色体隐性遗传(AR),常染色体显遗传(AD)和性连锁隐性遗传(XR),但散发病例亦不少见.本文对203例中日RP患者的遗传类型及并发症进行了总结分析.其中中国患者134例,AR占17.91%,AD占21.64%,XR占2.24%.散发者占58.21%.日本患者69例,AR占28.99%,AD占1.45%,XR占4.35%,散发者占65.21%.其发病年龄中位数为17.4岁,XR和AD发病较AR及散发者早.关于RP的并发症以并发白内障(54.68%)、玻璃体混浊(43.84%)最常见,并发屈光不正次之(21.18%).亦可见有并发视网膜脱离者。 (中华眼底病杂志,1993,9:29-30)

    Release date:2016-09-02 06:35 Export PDF Favorites Scan
  • 结晶样视网膜变性二家系报告

    Release date:2016-09-02 05:52 Export PDF Favorites Scan
  • 视网膜色素变性合并青光眼5例

    本文报告了视网膜色素变性合并青光眼患者5例,其中男性2例,女性3例。视网膜色素变性的发病年龄为15~33岁,平均年龄为20.8岁;青光眼的发病年龄23~51岁,平均年龄37.6岁;青光眼的类型:闭角型青光眼4例,开角型青光眼1例。本文就视网膜色素变性的遗传及视网膜色素变性合并青光眼的发病机理等问题进行了讨论。 (中华眼底病杂志,1992,8:183-184)

    Release date:2016-09-02 06:36 Export PDF Favorites Scan
  • OBSERVATION ON THE RETINAL HISTOPATHOLOGY AND 1TS ULTRASTRUCTURE IN A PATIENT WITH RETINITIS PIGMENTOSA.

    PURPOSE:To study the retinal pathologic changes and pathogenesis of relinhis pigmenlosa(RP). METHODS:The relina from a patient with autosomal dominant RP was examined by light and electron microscopy. RESULTS:Degeneration and structure disturbance almost involved in every layer of retina and were accompanied hy regional differenecs:Posterior region was more than periphery one in severity. Degeneration of retinal pigment epithelium(RPE)closely eorrelaled to that of the phmoreceplor. The uhraslrneture of the retina showed extensive and severe degeneration in the photoreeeptors ,particularly ill omer segments and mitoehondrlas. Lipofusein gramdes were accumuhtted in the cytoplagm. CONClUSIONS:These changes suggested that self-energizing system and self engulfing system of the photoreceptols were disfunctloned. (Chin J Ocul Fundus Dis,1997,13: 24-26)

    Release date:2016-09-02 06:12 Export PDF Favorites Scan
  • 原发性视网膜色素变性合并玻璃体囊肿

    本文报告3例原发性视网膜色素变性合并玻璃体囊肿,2例为双眼,1例为单眼。作者认为囊肿的发生,与视网膜、玻璃体变形有关。(中华眼底病杂志,1992,8:181-182)

    Release date:2016-09-02 06:36 Export PDF Favorites Scan
  • 伴视网膜血管增生性肿瘤和视网膜星形细胞错构瘤的Usher综合症1例

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  • 环形视网膜色素变性

    报告1例环形视网膜色素变性病人,其临床特征为双眼环绕黄斑的带状色素变性区.视力正常,无夜盲症状,眼底荧光血管造影显示病变区有视网膜色素上皮和脉络膜毛细血管萎缩.结合文献对本病的临床特点、眼底荧光血管造影及鉴别诊断进行简要讨论。 (中华眼底病杂志,1993,9:109-109)

    Release date:2016-09-02 06:35 Export PDF Favorites Scan
  • 单眼原发性视网膜色素变性4例报告

    报告4例单眼原发性视网膜色素变性病例.视野、暗适应、眼底荧光血管造影及ERG电生理检查均提示单眼患病之特征。并对本病的诊断、鉴别诊断及发病原因作一简要讨论。 (中华眼底病杂志,1993,9:39-40)

    Release date:2016-09-02 06:35 Export PDF Favorites Scan
  • 视网膜色素变性作外直肌脉络膜上腔移植术视网膜破孔二例

    报告2例视网膜色素变性患者,均在作一眼外直肌脉络膜上腔移植术时,引起视网膜膜破孔,经电凝修复.分别于5年和2年后随访,1例视网膜病变和视功能继续恶化,另1例无改善. (中华眼底病杂志,1993,9:89-90)

    Release date:2016-09-02 06:35 Export PDF Favorites Scan
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