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进行性延髓麻痹伴耳聋:两例临床及病理研究

Progressive pontobulbar palsy with deafness: clinical and pathological study of two cases.

作者信息

Brucher J M, Dom R, Lombaert A, Carton H

出版信息

Arch Neurol. 1981 Mar;38(3):186-90. doi: 10.1001/archneur.1981.00510030080012.

Abstract

Among the hereditary affections of the nervous system associated with deafness, a rare condition called "progressive pontobulbar palsy with deafness" has been described. In this slowly progressive condition, hearing loss and vestibular are-flexia are almost always the first symptoms, occurring in late childhood or early adulthood. Only 18 cases-some sporadic, several familial-have been published without a full report of pathological findings. The clinical and pathological data of two new cases-one familial, one sporadic-are described here. There are differences from other forms of bulbar paralysis, lower motor neuron diseases, and some spinocerebellar hereditary affections. In view of the homochrony and homotypy in familial cases and the pathological findings, progressive pontobulbar palsy with deafness appears to be an abiotrophic process wih autosomal recessive inheritance.

摘要

在与耳聋相关的遗传性神经系统疾病中,有一种罕见的病症被称为“伴有耳聋的进行性脑桥延髓麻痹”。在这种缓慢进展的病症中,听力丧失和前庭反射消失几乎总是最早出现的症状,出现在儿童晚期或成年早期。仅有18例病例——有些是散发性的,有些是家族性的——被报道,但均未对病理结果进行完整报告。本文描述了两例新病例的临床和病理数据,一例为家族性,一例为散发性。它与其他形式的延髓麻痹、下运动神经元疾病以及一些脊髓小脑遗传性疾病存在差异。鉴于家族性病例中的同步性和同型性以及病理结果,伴有耳聋的进行性脑桥延髓麻痹似乎是一种具有常染色体隐性遗传的营养障碍性过程。

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