%0 Journal Article
%A Lapp, Hanna Sophie
%A Günther, René
%T SOD1-ALS mimicking an inflammatory neuropathy: a case report.
%J Amyotrophic lateral sclerosis & frontotemporal degeneration
%V 26
%N 5-6
%@ 2167-8421
%C Abingdon
%I Taylor Francis Group
%M DZNE-2025-00888
%P 591 - 594
%D 2025
%X We present the case of a 36-year-old patient with a rapidly progressing SOD1-ALS, who was initially diagnosed as inflammatory acute motor axonal neuropathy due to contrast-enhancement of the lumbar spinal cord and a pure secondary motor neuron phenotype. Since the initiation of tofersen, disease progression and neurofilament levels impressively declined.
%K Humans
%K Adult
%K Amyotrophic Lateral Sclerosis: genetics
%K Amyotrophic Lateral Sclerosis: diagnosis
%K Diagnosis, Differential
%K Male
%K Superoxide Dismutase-1: genetics
%K Disease Progression
%K ALS (Other)
%K Amyotrophic lateral sclerosis (Other)
%K MRI (Other)
%K SOD1 mutation (Other)
%K contrast enhancement (Other)
%K Superoxide Dismutase-1 (NLM Chemicals)
%K SOD1 protein, human (NLM Chemicals)
%F PUB:(DE-HGF)16
%9 Journal Article
%$ pmid:40219902
%R 10.1080/21678421.2025.2488296
%U https://pub.dzne.de/record/280051