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101 Possible Causes for Amyotrophic Lateral Sclerosis, Facial Muscle Weakness and Progressive Atrophy, Muscular Atrophy

  • Amyotrophic Lateral Sclerosis

    The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] Frontotemporal white matter changes in amyotrophic lateral sclerosis.[ncbi.nlm.nih.gov]

  • Progressive Muscular Atrophy

    The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[en.wikipedia.org] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] Abstract Serum and CSF from 48 patients with amyotrophic lateral sclerosis and six patients with late-onset postpoliomyelitis progressive muscular atrophy were investigated[ncbi.nlm.nih.gov]

  • Spinal Muscular Atrophy

    […] muscle atrophy survival motor neuron spinal muscular atrophy spinal muscular atrophies of childhood Spinal muscular atrophy Statements spinal-muscular-atrophy-pro Identifiers[wikidata.org] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Because of retained tendon reflexes an atypical course of juvenile amyotrophic lateral sclerosis (ALS4) was considered.[ncbi.nlm.nih.gov]

  • Adult Spinal Muscular Atrophy

    […] spinal muscular atrophy and juvenile asymmetric segmental spinal muscular atrophy.[symptoma.com] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] J Neurol Sci. 324(1-2) 163-166 2013 [Refereed] Books etc Plain Text Genetics of amyotrophic lateral sclerosis : an overview.(共著) Amyotrophic Lateral Sclerosis.[researchmap.jp]

  • Motor Neuron Disease

    Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[ninds.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] lateral sclerosis/motor neuron disease patients or their caregivers and (iv) the population sample included patients of amyotrophic lateral sclerosis/motor neuron disease[ncbi.nlm.nih.gov]

  • Multifocal Motor Neuropathy

    Abstract Multifocal motor neuropathy (MMN) and progressive muscular atrophy (PMA) are associated with IgM monoclonal gammopathy or the presence IgM anti-GM1-antibodies.[ncbi.nlm.nih.gov] In the first patient the symptoms were slowly progressive with bulbar muscle impairment, generalized weakness, muscular atrophy with cramps and fasciculations.[moh-it.pure.elsevier.com] The spinal cord, however, revealed severe neuronal loss in the ventral horn and axonal loss in the corticospinal tract, indicative of amyotrophic lateral sclerosis.[ncbi.nlm.nih.gov]

  • Myotonic Dystrophy

    Neuromuscular disorders like myotonic dystrophy (dystrophia myotonica or Steinert's disease) and spinal muscular atrophy are associated with perioperative complications related[ncbi.nlm.nih.gov] Clinical Presentation: Variable, progressive disability; facial and distal limb muscle weakness with myotonia; cataracts; cardiac conduction defects; diabetes mellitus; and[ajnr.org] Lateral Sclerosis (ALS), the most common Neuromuscular Diseases in the adult age.[ncbi.nlm.nih.gov]

  • Progressive Bulbar Palsy

    […] term(s): Adult form spinal muscular atrophy Childhood form, type II spinal muscular atrophy Distal spinal muscular atrophy Juvenile form, type III spinal muscular atrophy[icd10coded.com] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[secure.ssa.gov] Motor Neuron Disease (or ‘amyotrophic lateral sclerosis’, ALS). ‘’Brain Damage, Brain Repair.’’[en.wikipedia.org]

  • Spinal and Bulbar Muscular Atrophy

    KEYWORDS: CAG/polyglutamine expansion; androgen receptor; neuromuscular disease; spinal and bulbar muscular atrophy; testosterone[ncbi.nlm.nih.gov] Abstract Spinal and bulbar muscular atrophy (SBMA) is the first member identified among polyglutamine diseases characterized by slowly progressive muscle weakness and atrophy[ncbi.nlm.nih.gov] INTRODUCTION: Spinal and bulbar muscular atrophy (SBMA) and amyotrophic lateral sclerosis (ALS) are motor neuron diseases.[ncbi.nlm.nih.gov]

  • Upper Motor Neuron Disease

    atrophy(PMA), Progressive bulbar palsy(PBP), MEPs were recorded from abductor pollicis brevis and abductor hallucis.[e-acn.org] Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com] OBJECTIVE: To assess the relationship between clinically assessed Upper Motor Neuron (UMN) disease in Amyotrophic Lateral Sclerosis (ALS) and local diffusion alterations measured[ncbi.nlm.nih.gov]

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