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.