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908 Possible Causes for EMG Shows Neurogenic Abnormalities, Facial Muscle Weakness and Progressive Atrophy, Myoclonic Jerking

  • Amyotrophic Lateral Sclerosis

    EMG change were at an earlier stage of evolution than those showing severe weakness and marked neurogenic EMG change.[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] ) Males symptomatic; slowly progressive bulbar and limb weakness Family history; fasciculations of facial muscles; gynaecomastia; proximal symmetrical weakness in addition[doi.org]

  • 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: Myoclonic Jerking
  • 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: Myoclonic Jerking
  • 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: Myoclonic Jerking
  • 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: Myoclonic Jerking
  • Hypoglycemia

    In newborns, hypoglycemia can produce irritability, jitters, myoclonic jerks, cyanosis, respiratory distress, apneic episodes, sweating, hypothermia, somnolence, hypotonia[en.wikipedia.org]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Acute Amphetamine Intoxication

    jerks Twitching Choreiform movements 3.[clinicaladvisor.com] Hallucinations Integumentary Diaphoresis Bruising and injuries Track marks Abscess Excoriation Gastrointestinal Abdominal pain Nausea/Vomiting Musculoskeletal Muscle rigidity Myoclonic[clinicaladvisor.com]

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

    After 36 hours of donepezil remission, the frequency of the myoclonic jerks was sharply reduced. The patient remains asymptomatic after 6 months of follow-up.[ncbi.nlm.nih.gov]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Restless Legs Syndrome

    Restless legs syndrome (Willis-Ekbom disease) is a neurological disorder characterized by an urge to move the limbs, paresthesias, motor restlessness and worsening of symptoms by relaxation. It most commonly affects the legs. Affected individuals complain of restlessness, feeling of unpleasant sensation in their legs[…][symptoma.com]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Acute Renal Failure

    Such symptoms include Anorexia Nausea Vomiting Weakness Myoclonic jerks Seizures Confusion Coma Asterixis and hyperreflexia may be present on examination.[merckmanuals.com] Later, as nitrogenous products accumulate, symptoms of uraemia may develop, including anorexia, nausea and vomiting, weakness, myoclonic jerks, seizures, confusion, and coma[web.archive.org]

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