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[多伊内黄斑遗传性营养不良与良性单克隆丙种球蛋白病。遗传与发病机制的相关性(作者译)]

[Doyne's macular heredodystrophy and benign monoclonal gammopathy. Genetic and pathogenetic correlations (author's transl)].

作者信息

Munteanu G

出版信息

J Fr Ophtalmol. 1980 Dec;3(12):753-8.

PMID:7217618
Abstract

Doyne's macular heredodystrophy associated with benign monoclonal gammopathy was seen in 4 patients having genetic correlations in 3 generations. One case showed crystalline stromal corneal deposits. Based on this pathological association and the morphofunctional support of the pair, choriocapillaris Bruch's membrane, Doyne's macular heredodystrophy is considered as a symptom of the immunoglobulin deficiency syndrome (IgM). The pathogenicity of Doyne's macular dystrophy and of the secondary drusen is interpreted as a dynamic phenomenon related to all the morphofunctional changes occurring at the level of the choriocapillaris Bruch's membrane, and the pigmented epithelium.

摘要

多伊内黄斑遗传性营养不良伴良性单克隆丙种球蛋白病在3代有遗传相关性的4例患者中被发现。1例患者出现角膜基质结晶样沉积物。基于这种病理关联以及脉络膜毛细血管-布鲁赫膜这一配对结构的形态功能支持,多伊内黄斑遗传性营养不良被认为是免疫球蛋白缺乏综合征(IgM)的一种症状。多伊内黄斑营养不良和继发性玻璃膜疣的致病性被解释为一种与脉络膜毛细血管-布鲁赫膜以及色素上皮水平发生的所有形态功能变化相关的动态现象。

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