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264 Possible Causes for EMG Shows Neurogenic Abnormalities, Facial Muscle Weakness and Progressive Atrophy, Grip Strength Decreased

  • Amyotrophic Lateral Sclerosis

    EMG change were at an earlier stage of evolution than those showing severe weakness and marked neurogenic EMG change.[doi.org] Prior animal studies have shown that silencing SOD1 led to preservation of grip strength and a delay in the onset of motor function deficits [ 125, 126 ].[doi.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]

  • Motor Neuron Disease

    Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] Progressive bulbar palsy , also called progressive bulbar atrophy, involves the brain stem—the bulb-shaped region containing lower motor neurons needed for swallowing, speaking[ninds.nih.gov] Progressive bulbar palsy, also called progressive bulbar atrophy, involves the brain stem—the bulb-shaped region containing lower motor neurons needed for swallowing, speaking[web.archive.org]

    Missing: EMG Shows Neurogenic Abnormalities
  • Distal Spinal Muscular Atrophy Type 3

    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] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info] They all result in progressive lower motor neurone weakness. The gene defect is on chromosome 5q and the implicated gene is called survival motor neurone gene 1 (SMN1).[patient.info]

    Missing: Grip Strength Decreased
  • Myotonic Dystrophy

    Clinical Presentation: Variable, progressive disability; facial and distal limb muscle weakness with myotonia; cataracts; cardiac conduction defects; diabetes mellitus; and[ajnr.org] The clinical course led progressively to major disability with severe proximal weakness and atrophy and, later on, distal weakness, atrophy and neck extensor weakness responsible[doi.org] , in males, testicular atrophy Key Diagnostic Features: MRI features: Subcortical hyperintensity of the white matter on T2-weighted sequences, with a predilection for the[ajnr.org]

    Missing: EMG Shows Neurogenic Abnormalities
  • Spinal Muscular Atrophy Type 1

    We present a baby with spinal muscular atrophy type 1, an inherited disorder causing progressive weakness, leading to complete paralysis of respiratory, facial and limb muscles[ncbi.nlm.nih.gov] 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] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info]

    Missing: Grip Strength Decreased
  • Spinal Muscular Atrophy Type 4

    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] Scapuloperoneal spinal muscular atrophy: Type 1 (AD form) appears at age 14-26, with weakness, distal leg atrophy, and absent tendon reflexes and sparing of intrinsic foot[emedicine.medscape.com] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info]

    Missing: Grip Strength Decreased
  • Spinal Muscular Atrophy Type 2

    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] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info] They all result in progressive lower motor neurone weakness. The gene defect is on chromosome 5q and the implicated gene is called survival motor neurone gene 1 (SMN1).[patient.info]

    Missing: Grip Strength Decreased
  • Lambert Eaton Myasthenic Syndrome

    MuSK MG should be considered if there is facial or tongue weakness with atrophy, or weakness that predominates in neck or shoulder muscles.[docksci.com] MG follows a variable course, but usually progresses.[docksci.com]

    Missing: EMG Shows Neurogenic Abnormalities
  • Carpal Tunnel Syndrome

    There was a significant (t10 5.45, P 0.001) 37% decrease in grip strength immediately following surgery.[ncbi.nlm.nih.gov] Post-operatively the patient is likely to experience scar tenderness and decreased grip strength for a few months and may require several weeks off work.[apps.nhslothian.scot] As symptoms worsen, people might feel tingling during the day, and decreased grip strength may make it difficult to form a fist, grasp small objects, or perform other manual[web.archive.org]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • De Quervain Tenosynovitis

    Impairments include pain over the first compartment of the wrist, decreased wrist and finger ROM and joint mobility, decreased grip strength, and difficulty grasping objects[thestudentphysicaltherapist.com] Patients typically report painful abduction of the thumb and decreased grip strength. [4] The most common cause is chronic overuse.[physio-pedia.com] […] in grip strength. 1 - 4 Characteristics of de Quervain tenosynovitis are shown in Figure 1.[jaoa.org]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy

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