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通过光学显微镜和电子显微镜观察的Usher综合征内耳组织病理学。

Histopathology of the inner ear in Usher's syndrome as observed by light and electron microscopy.

作者信息

Shinkawa H, Nadol J B

出版信息

Ann Otol Rhinol Laryngol. 1986 May-Jun;95(3 Pt 1):313-8. doi: 10.1177/000348948609500321.

Abstract

A case of Usher's syndrome, type 3, is described. Histologic study of the inner ear of the patient demonstrated hair cell loss in the basal turn, severe loss of spiral ganglion cells, widespread neural degeneration in the cochlea, and discrete collections of degenerating supporting cells in the organ of Corti. The pattern of neural degeneration bore some similarity to abnormalities in the retina in retinitis pigmentosa. However, the findings in the supporting cells had no obvious parallel to the findings in the retina in this disorder. The histopathology of Usher's syndrome has been equated with the Scheibe, or cochleosaccular, pattern of degeneration. However, the findings in the present case and a critical analysis of published data did not support this concept.

摘要

本文描述了一例3型Usher综合征病例。对该患者内耳的组织学研究显示,基底转毛细胞缺失,螺旋神经节细胞严重丢失,耳蜗广泛神经变性,以及柯蒂器中支持细胞的离散性退变聚集。神经变性模式与色素性视网膜炎视网膜异常有一定相似性。然而,支持细胞的这些发现与该疾病视网膜的发现并无明显相似之处。Usher综合征的组织病理学已等同于Scheibe型或耳蜗球囊型退变模式。然而,本病例的发现以及对已发表数据的批判性分析并不支持这一概念。

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