Pathology in a case of profound congenital deafness
Pathology in a case of profound congenital deafness
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DOI：
10.1017/s0022215100077860
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发表时间：
1973-10
期刊：
影响因子：
--
通讯作者：
H. Schuknecht;J. L. Wright
中科院分区：
文献类型：
--
作者：
H. Schuknecht;J. L. Wright
所有研究过人耳病理学的人都知道，将形态学变化与听觉和前庭功能障碍联系起来是困难的。这是特别明显的，当很长的时间跨度分开的日期发病的耳科疾病和死亡的个人。关于病因和发病机制的假设通常是更有效的病理标本时，可从几个人与一个可疑的共同的临床实体;然而，一个单一的病例报告，有时可以提供有用的信息，为其他从事类似的研究。因此，我们希望报告的病理结果的情况下，深刻的“先天性”耳聋。
ALL who have studied human ear pathology know the difficulties encountered in correlating morphological changes with auditory and vestibular dysfunction. This is particularly evident when long time-spans separate the date of onset of otological disease and death of the individual. Assumptions regarding etiology and pathogenesis are usually more valid when pathological specimens are available from several individuals with a suspected common clinical entity; however, a single case report can sometimes provide useful information for others engaged in similar studies. We wish, therefore, to report the pathological findings in a case of profound 'congenital' deafness.