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431 Possible Causes for Motor Neuron Disease, Spinal Cord Atrophy

  • Muscular Atrophy

    Neurogenic causes of muscle atrophy :  Multiple sclerosis (disease that affects the brain and spinal cord causing weakness, coordination, balance difficulties, and other[] Simultaneous hereditary polyneuropathy and motor neuron disease were suspected and relevant genetic testing was confirmed HNPP and SBMA.[] neuron disease G12.21 Amyotrophic lateral sclerosis G12.22 Progressive bulbar palsy G12.23 Primary lateral sclerosis G12.24 Familial motor neuron disease G12.25 Progressive[]

  • Progressive Muscular Atrophy

    This disorder is defined as a hereditary familial degeneration of the motor cells in the anterior horns of the spinal cord causing progressive atrophy and paralysis of the[] Because the upper motor neurons are not involved, those suffering from PMA may often not experience the muscular stiffness or the loss of emotional control which Motor Neurone[] There was complete resolution of the abnormal brain MRI lesions; however, the cervical spinal cord MRI lesion and muscular atrophy remained unchanged.[]

  • Spinal Muscular Atrophy

    Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder pathologically characterized by the degeneration of motor neurons in the spinal cord and muscle atrophy[] neuron disease; NAA/Cr; SMA; Spinal muscular atrophy; TE; TSD; TSE; Tay–Sachs disease; amyotrophic lateral sclerosis; fluorodeoxyglucose positron emission tomography; hexosaminidase[] Clinical Information A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without[]

  • Adult Spinal Muscular Atrophy

    Definition A form of spinal muscular atrophy, a neuromuscular disorder characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical[] Electrophysiological studies showed patterns of lower motor neuron disease and genetic test showed P56S mutation of VAPB gene.[] What is spinal muscular atrophy adult type? Spinal Muscular Atrophy Adult Type is a condition that affects the nerve cells (motor neurons) in your spinal cord.[]

  • Spinal Muscular Atrophy Type 3

    Abstract Proximal spinal muscular atrophy (Kugelberg-Welander syndrome) is a degenerating disease of the anterior horn cells of the spinal cord with atrophy of the proximal[] Neuron Disease Experiencing Muscle Cramps. 22nd June 2017 Condition : Motor Neuron Disease Interventions : Drug: FLX-787-ODT (orally disintegrating tablet); Drug: Placebo[] Spinal musular atrophies are a group of genetic disorders distinguished by progressive degeneration of anterior horn cells in the spinal cord.[]

  • Spinal and Bulbar Muscular Atrophy

    […] muscular atrophy (SBMA).[] Mazen Dimachkie lead this publication on Motor Neuron Disease.[] KEYWORDS: Kennedy's disease; craniofacial; genetics; motor neuron disease; spinal and bulbar muscular atrophy; weakness[]

  • Amyotrophic Lateral Sclerosis

    Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register.[] ALS (amyotrophic lateral sclerosis) is a degenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brainstem and spinal cord.[] ALS causes the degeneration of both the upper motor neurons in the brain and the lower motor neurons in the spinal cord.[]

  • Spinal Muscular Atrophy Type 1

    The association of diseases within this family suggests that chromosome 5q should also be studied in relation to adult-onset familial motor neuron disease.[] Spinal Muscular Atrophy Type 1 is an inherited (genetic) condition that affects the nerve cells (motor neurons) in your spinal cord.[] CONTEXT: Spinal muscular atrophy type 1, an autosomal recessive motor neuron disease, is a leading genetic cause of death in infancy and early childhood.[]

  • Primary Lateral Sclerosis

    The spinal cord and nerve roots appeared normal.[] Living With a Motor Neuron Disease The outlook is different for each type of motor neuron disease. Some are milder and progress more slowly than others.[] In the present study, the distribution and severity, and biochemical profile of phosphorylated TDP-43 (pTDP-43) in the brains and spinal cords were examined immunohistochemically[]

  • Progressive Bulbar Palsy

    Progressive muscular atrophy is a variety of ALS in which the neuron degeneration is most pronounced in the spinal cord.[] Abstract A case is presented of a patient with progressive bulbar palsy, a form of motor neuron disease, which is a progressive degenerative disorder of the motor nuclei in[] Motor Neuron Disease: Classification and nomenclature. ALS and Other Motor Neuron Disorders. 1:105-112. (2000) Kadekawa J et al.[]

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