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314 Possible Causes for EMG Shows Neurogenic Abnormalities, Facial Muscle Weakness and Progressive Atrophy, Loss of Spinal Anterior Horn Cells

  • Spinal Muscular Atrophy Type 1

    In pathologic terms, the disease was characterized by loss of anterior horn cells.[emedicine.medscape.com] 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]

  • Distal Spinal Muscular Atrophy Type 3

    In pathologic terms, the disease was characterized by loss of anterior horn cells.[emedicine.medscape.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] Clinical Features (general for all types of SMA) Progressive degeneration and loss of the lower motor neurons (anterior horn cells) in the spinal cord and sometimes in the[slideshare.net]

  • Spinal Muscular Atrophy Type 4

    In pathologic terms, the disease was characterized by loss of anterior horn cells.[emedicine.medscape.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] […] of the anterior horn cells in the spinal cord and the brain stem nuclei.[omicsonline.org]

  • Spinal Muscular Atrophy Type 2

    In pathologic terms, the disease was characterized by loss of anterior horn cells.[emedicine.medscape.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] Available from: » Introduction Proximal spinal muscular atrophy (SMA) is a genetically heterogeneous disease with paresis and muscle atrophy due to loss of anterior horn cell[neurologyindia.com]

  • Amyotrophic Lateral Sclerosis

    EMG change were at an earlier stage of evolution than those showing severe weakness and marked neurogenic EMG change.[doi.org] A loss of motor cells in the anterior horns of the spinal cord is reflected in the deterioration of manual dexterity in ALS patients. 2.[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]

  • Distal Hereditary Motor Neuropathy Type 2

    […] of motor neuron cells in the anterior horn of the spinal cord and subsequent muscle atrophy.[en.wikipedia.org] weakness DHMN8 600175 TRPV4 12q24.11 Autosomal dominant Congenital distal spinal muscular atrophy Affects primarily distal muscles of lower limbs, non-progressive, rare DHMNJ[en.wikipedia.org] […] are a genetically and clinically heterogeneous group of motor neuron diseases that result from genetic mutations in various genes and are characterized by degeneration and loss[en.wikipedia.org]

  • Spinal Muscular Atrophy

    Spinal muscular atrophy: A genetic disease characterized by progressive loss of lower motor neurons (anterior horn cells) in the spinal cord, resulting in symmetric muscle[medicinenet.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] Muscle atrophy, caused by a progressive loss of the anterior horn cells in the spinal cord, is universal.[emedicine.medscape.com]

    Missing: EMG Shows Neurogenic Abnormalities
  • Distal Hereditary Motor Neuropathy Type 2A

    […] of motor neuron cells in the anterior horn of the spinal cord and subsequent muscle atrophy.[en.wikipedia.org] weakness DHMN8 600175 TRPV4 12q24.11 Autosomal dominant Congenital distal spinal muscular atrophy Affects primarily distal muscles of lower limbs, non-progressive, rare DHMNJ[en.wikipedia.org] […] are a genetically and clinically heterogeneous group of motor neuron diseases that result from genetic mutations in various genes and are characterized by degeneration and loss[en.wikipedia.org]

  • Adult Spinal Muscular Atrophy

    Muscle atrophy, caused by a progressive loss of the anterior horn cells in the spinal cord, is universal.[emedicine.medscape.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] horn cells (the lower motor neurons) in the spinal cord and the brain stem nuclei.[genomicseducation.hee.nhs.uk]

    Missing: EMG Shows Neurogenic Abnormalities
  • Fingerprint Body Myopathy

    The EMG shows firing of motor units, reflecting an origin from spontaneous neural discharge.[basicmedicalkey.com] Within few years the disease progressed to generalized muscle weakness and atrophy, ptosis, ophthalmoplegia externa and areflexia.[scipers.com] On occasion, disorders affecting the motor nerve cell bodies in the spinal cord (anterior horn cell disease), the neuromuscular junction, or peripheral nerves can mimic findings[basicmedicalkey.com]