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192 Possible Causes for Muscular Atrophy, Severe Peripheral Motor Neuropathy

  • Peripheral Neuropathy

    We treated a 52-year-old man who had severe disabling classic peripheral neuropathy since 1998 with Scrambler Therapy (Calmare), an FDA-cleared peripheral non-invasive neuromodulation[] Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[] Boulis works on novel treatments for several nerve disorders, including Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease) and Spinal Muscular Atrophy[]

  • Polyneuropathy

    Neuronal Peroneal Muscular Atrophy (HMSN II) Autosomal dominant inheritance is also the case with HMSN II.[] Disease process involving several peripheral nerves (literal sense). 2.[] Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy. Hum. Mol.[]

  • Motor Neuron Disease

    In recent years, several reports show association of HIV infection with Amyotrophic Lateral Sclerosis - Syndrome, Motor Neuron Diseases and peripheral neuropathies.[] Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[] Several conditions have been reported to mimic motor neuron disease (MND) and misdiagnosis remains a common clinical problem.[]

  • 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.[] An autopsy showed severe widespread demyelination without lymphoma cell infiltration in the peripheral nerves.[] Monoclonal gammopathy was determined by immunoelectrophoresis and immunofixation in serum from 445 patients with ALS, 158 patients with progressive muscular atrophy (PMA),[]

  • Charcot Marie Tooth Disease

    Charcot-Marie Tooth disease (CMT) encompasses several inherited peripheral motor-sensory neuropathies and is one of the most common inherited neuromuscular diseases.[] 2015 ICD-9-CM Diagnosis Code 356.1 Peroneal muscular atrophy 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 356.1 is a billable medical code that[] STATE OF THE ART REVIEW First Online: 09 February 2007 Abstract Charcot-Marie Tooth disease (CMT) encompasses several inherited peripheral motor-sensory neuropathies and is[]

  • Hereditary Motor and Sensory Neuropathy

    Charcot-Marie-Tooth disease Déjérine-Sottas disease Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal[] Abstract Hereditary motor and sensory neuropathies (HMSN) are genetically heterogeneous disorders affecting peripheral motor and sensory functions.[] It results in severe demyelination with delayed motor skills and is much more severe than type 1.[]

  • Diabetic Neuropathy

    View/Print Table TABLE 2 Symptoms of Diabetic Neuropathy Sensorimotor neuropathy Muscular symptoms: muscle weakness (not fatigue), atrophy, balance problems, ataxic gait Sensory[] Diabetic neuropathy affects all peripheral nerves including sensory neurons, motor neurons, but rarely affects the autonomic nervous system.[] […] symptoms: muscle weakness (not fatigue), atrophy, balance problems, ataxic gait Sensory symptoms: pain, paresthesia, numbness, paralysis, cramping, nighttime falls, antalgic[]

  • Guillain-Barré Syndrome

    RESULTS: All six patients had different degrees of muscular atrophy at nadir and in two, respiratory muscles were involved.[] Acute Motor Axonal Neuropathy (AMAN) No sensory deficits Associated with epidemics following C. jejuni enteritis.[] The peroneal muscular atrophy syndrome 8. The ataxic neuropathies 9. Sensory neuropathies 10. Neuropathies in metabolic and degenerative disorders 11.[]

  • Transverse Myelitis

    Doug was the global lead for a series of programs in Alzheimer’s disease, Amyotrophic Lateral Sclerosis (ALS) and Spinal Muscular Atrophy (SMA).[] (AMAN, more rapidly evolving and more severe motor deficits, no sensory deficits), acute motor and sensory axonal neuropathy (AMSAN, reported nearly exclusively in adults[] ), Miller-Fisher syndrome (ataxia, ophthalmoplegia, and areflexia without peripheral weakness), pharyngeal-cervical-brachial motor variant (ptosis, facial, pharyngeal, neck[]

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    Several subtypes of inherited peripheral neuropathies were delineated and classified as hereditary motor and sensory neuropathies (HMSN), hereditary motor neuropathies (HMN[] […] are not associated with a defect in the SMN1 gene on chromosome 5q X-linked spinal muscular atrophy X-linked spinal muscular atrophy is seen only among males![] Diseases of the peripheral nerves (peripheral neuropathies, or polyneuropathies ) can produce symptoms similar to the motor neuron diseases.[]

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