Literature DB >> 28434507

Motor neuropathies and lower motor neuron syndromes.

A Verschueren1.   

Abstract

Motor or motor-predominant neuropathies may arise from disease processes affecting the motor axon and/or its surrounding myelin. Lower motor neuron syndrome (LMNS) arises from a disease process affecting the spinal motor neuron itself. The term LMNS is more generally used, rather than motor neuronopathy, although both entities are clinically similar. Common features are muscle weakness (distal or proximal) with atrophy and hyporeflexia, but no sensory involvement. They can be acquired or hereditary. Immune-mediated neuropathies (multifocal motor neuropathy, motor-predominant chronic inflammatory demyelinating polyneuropathy) are important to identify, as effective treatments are available. Other acquired neuropathies, such as infectious, paraneoplastic and radiation-induced neuropathies are also well known. Focal LMNS is an amyotrophic lateral sclerosis (ALS)-mimicking syndrome especially affecting young adults. The main hereditary LMNSs in adulthood are Kennedy's disease, late-onset spinal muscular atrophy and distal hereditary motor neuropathies. Motor neuropathies and LMNS are all clinical entities that should be better known, despite being rare diseases. They can sometimes be difficult to differentially diagnose from other diseases, particularly from the more frequent ALS in its pure LMN form. Nevertheless, correct identification of these syndromes is important because their treatment and prognoses are definitely different.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  ALS; Benign monomelic amyotrophy; Lower motor neuron syndrome; Motor neuronopathy; Motor neuropathy; Spinal muscular atrophy

Mesh:

Year:  2017        PMID: 28434507     DOI: 10.1016/j.neurol.2017.03.018

Source DB:  PubMed          Journal:  Rev Neurol (Paris)        ISSN: 0035-3787            Impact factor:   2.607


  5 in total

1.  A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report.

Authors:  Juanjuan Chen; Jun Wu; Chunxi Han; Yao Li; Yuzu Guo; Xiaoxin Tong
Journal:  BMC Neurol       Date:  2019-08-17       Impact factor: 2.474

2.  Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy.

Authors:  Daojun Hong; Pu Fang; Sheng Yao; Juanjuan Chen; Xiaolei Zhang; Shuyun Chen; Jingfen Zhang; Dandan Tan; Li Wang; Xinsheng Han; Ling Xin; Yan Wang; Meige Liu; Lu Cong; Shanshan Zhong; Hui Ouyang; Xuguang Gao; Jun Zhang
Journal:  Ann Clin Transl Neurol       Date:  2019-08-20       Impact factor: 4.511

3.  Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy.

Authors:  Chengsi Wu; Haijie Xiang; Ran Chen; Yilei Zheng; Min Zhu; Shuyun Chen; Yanyan Yu; Yun Peng; Yaqing Yu; Jianwen Deng; Meihong Zhou; Daojun Hong
Journal:  Ann Clin Transl Neurol       Date:  2022-03-17       Impact factor: 5.430

Review 4.  Purinergic Receptors in Neurological Diseases With Motor Symptoms: Targets for Therapy.

Authors:  Ágatha Oliveira-Giacomelli; Yahaira Naaldijk; Laura Sardá-Arroyo; Maria C B Gonçalves; Juliana Corrêa-Velloso; Micheli M Pillat; Héllio D N de Souza; Henning Ulrich
Journal:  Front Pharmacol       Date:  2018-04-10       Impact factor: 5.810

5.  Pediatric Motor Inflammatory Neuropathy: The Role of Antiphospholipid Antibodies.

Authors:  Claudia Brogna; Marco Luigetti; Giulia Norcia; Roberta Scalise; Gloria Ferrantini; Beatrice Berti; Domenico M Romeo; Raffaele Manna; Eugenio Mercuri; Marika Pane
Journal:  Brain Sci       Date:  2020-03-07
  5 in total

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