Lombaert A, Dom R, Carton H, Bruchler J M
Acta Neurol Belg. 1976;76(5-6):309-14.
Progressive ponto-bulbar palsy with deafness is a rare disease. It seems to be an abiotrophic process with autosomal recessive inheritance in most instances. Only one autopsy case had been briefly described (Lelong et al., 1941). The clinical features and the pathological findings of a new case are reported. The structures primarily involved are the grey matter of the brain stem and the spinal cord, including to some extent the optic tracts and most of the fiber tracts in the brain stem with exception of the pyramidal tracts.
进行性脑桥延髓麻痹伴耳聋是一种罕见疾病。在大多数情况下,它似乎是一种具有常染色体隐性遗传的营养障碍性过程。仅一篇尸检病例曾被简要描述(勒隆等人,1941年)。本文报告了一例新病例的临床特征和病理发现。主要受累结构是脑干和脊髓的灰质,在一定程度上还包括视束以及脑干中除锥体束外的大多数纤维束。