Literature DB >> 27224438

Case of Young-Onset Sporadic Amyotrophic Lateral Sclerosis.

Artemios K Artemiadis1, Christos Peppas, Sotiris Giannopoulos, Vasiliki Zouvelou, Nikos Triantafyllou.   

Abstract

Amyotrophic lateral sclerosis (ALS) constitutes the main type of motor neuron disease. Familial ALS is characterized by the presence of positive family history and accounts for 10% of ALS cases. Although familial ALS is the main culprit for early-onset disease, there are rare cases of early- or young-onset ALS with negative family history or sporadic ALS. We describe a 23-year-old man with clinical and electrophysiological evidence of probable sporadic ALS according to the revised EI Escorial criteria. Interestingly, brain neuroimaging revealed bilaterally increased T2 signals across corona radiata, posterior limb of the internal capsule, and descending motor tracts in the brainstem and hypointensity rim of the motor cortex on T2-weighted images. Young-onset sporadic ALS may be a distinct nosological entity. The topic is shortly discussed in the light of its genetic and clinical characteristics.

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Year:  2016        PMID: 27224438     DOI: 10.1097/CND.0000000000000107

Source DB:  PubMed          Journal:  J Clin Neuromuscul Dis        ISSN: 1522-0443


  2 in total

1.  Fulminant amyotrophic lateral sclerosis manifesting in a young woman during pregnancy.

Authors:  Yuliia Solodovnikova; Anastasiia Kobryn; Alina Ivaniuk; Anatoliy Son
Journal:  Neurol Sci       Date:  2021-03-10       Impact factor: 3.307

Review 2.  From Multi-Omics Approaches to Precision Medicine in Amyotrophic Lateral Sclerosis.

Authors:  Giovanna Morello; Salvatore Salomone; Velia D'Agata; Francesca Luisa Conforti; Sebastiano Cavallaro
Journal:  Front Neurosci       Date:  2020-10-30       Impact factor: 4.677

  2 in total

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