Argyll-Robertson-Like Pupils in the Neural Type of Charcot-Marie-Tooth Disease
- 1 January 1977
- journal article
- research article
- Published by S. Karger AG in European Neurology
- Vol. 16 (1-6) , 172-175
- https://doi.org/10.1159/000114897
Abstract
Argyll-Robertson-like pupils were noted in 3 patients presenting the neural type of Charcot-Marie-Tooth (CMT) disease with peroneal muscular atrophy. Up to now the light-near dissociation was reported in the hypertrophic variety of CMT disease. The presence of the light-near dissociation in patients with CMT disease does not help in clinically differentiating the neural from the hypertrophic type of this disease.Keywords
This publication has 2 references indexed in Scilit:
- Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular AtrophyArchives of Neurology, 1968
- Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular AtrophyArchives of Neurology, 1968