Literature DB >> 1007898

Progressive ponto-bulbar palsy with deafness. A clinico-pathological study.

A Lombaert, R Dom, H Carton, J M Bruchler.   

Abstract

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.

Entities:  

Mesh:

Year:  1976        PMID: 1007898

Source DB:  PubMed          Journal:  Acta Neurol Belg        ISSN: 0300-9009            Impact factor:   2.396


  4 in total

1.  Recovery from respiratory muscle failure in a sporadic case of Brown-Vialetto-Van Laere syndrome with unusually late onset.

Authors:  G Piccolo; E Marchioni; M Maurelli; F Simonetti; F Bizzetti; F Savoldi
Journal:  J Neurol       Date:  1992-07       Impact factor: 4.849

2.  Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance.

Authors:  S A Hawkins; N C Nevin; A E Harding
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318

3.  Progressive bulbar paralysis in childhood: a case report.

Authors:  G F Perticoni; T A Cantisani; H Fisher
Journal:  Ital J Neurol Sci       Date:  1983-04

4.  Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings.

Authors:  Samira Yadegari; Askar Ghorbani; Mitra Ansari Dezfouli; Shahriar Nafissi
Journal:  Iran J Neurol       Date:  2011
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.