The sympathetic skin response (SSR) was evaluated in 25 patients with
amyotrophic lateral sclerosis (ALS) to assess for involvement of the a
utonomic nervous system. Twenty-two age-matched normals and 6 patients
with muscular dystrophy served as controls. The SSR was intact in all
normal volunteers and all patients with muscular dystrophy. The mean
SSR latency in the ALS patients was prolonged compared to that of norm
als (2.29 +/- 0.28 versus 2.13 +/- 0.16 s, P < 0.05). The SSR was abse
nt in one or both legs of 10 ALS patients (40%). Absence or abnormal l
atency of SSR in patients with ALS without clinical findings of autono
mic failure suggests involvement of the autonomic nervous s stem in ad
dition to the motor s tem. (C) 1993 John Wiley & Sons, Inc.