Analysis of sensory function in Charcot-Marie-Tooth disease

Citation
U. Ericson et K. Borg, Analysis of sensory function in Charcot-Marie-Tooth disease, ACT NEUR SC, 99(5), 1999, pp. 291-296
Citations number
17
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ACTA NEUROLOGICA SCANDINAVICA
ISSN journal
00016314 → ACNP
Volume
99
Issue
5
Year of publication
1999
Pages
291 - 296
Database
ISI
SICI code
0001-6314(199905)99:5<291:AOSFIC>2.0.ZU;2-8
Abstract
Ten patients each with Charcot-Marie-Tooth disease type 1 (CMT1), demyelina ting form, and CMT2, axonal form, were subjected to analysis of sensory fun ction including sensory screening and quantitative determination of thermal , thermal pain and vibratory thresholds in hands and feet. The threshold va lues were compared with data from age- and sex-matched control groups. All patients had a symmetrical sensory dysfunction, which was most prominent in the lower extremities. Temperature was the modality most often affected on screening and on quantitative determination of thresholds in both CMT1 and CMT2 patients. Mean thermal thresholds were significantly increased in bot h hands and feet in CMT1 as well as in CMT2 patients when compared with con trols. There was no statistically significant difference between thermal th resholds in the CMT1 and CMT2 patients. Mean thermal pain thresholds were s ignificantly increased in the feet of the CMT2 patients when compared with the controls and they were significantly higher in the hands of the CMT2 th an in the CMT1 patients. Vibratory thresholds (VT) were abnormal in all CMT 1 patients and in a majority of the CMT2 patients. Mean VT was significantl y increased in hands and feet of both CMT1 and CMT2 patients when compared with the controls and the mean VT was significantly higher in the feet of t he CMT1 than in the CMT2 patients. The difference with an increased heat pa in threshold in the CMT2 patients and an increased VT in the CMT1 patients is suggested to be due to demyelination in CMT1 leading to affection of sen sory function mediated by myelinated nerve fibres and to axonal disturbance in CMT2 with affection of sensory function mediated by small diameter myel inated and unmyelinated C-fibres.