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  2. Basal ganglia disease - Wikipedia

    en.wikipedia.org/wiki/Basal_ganglia_disease

    The basal ganglia is a collective group of structures in the brain. These include the striatum, (composed of the putamen and caudate nucleus), globus pallidus, substantia nigra, and the subthalamic nucleus. Along with other structures, the basal ganglia are part of a neural circuit that is integral to voluntary motor function. [1]

  3. Biotin-thiamine-responsive basal ganglia disease - Wikipedia

    en.wikipedia.org/wiki/Biotin-thiamine-responsive...

    Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare disease that affects the nervous system, particularly the basal ganglia in the brain. [4] It is a treatable neurometabolic disorder with autosomal recessive inheritance.

  4. Basal ganglia - Wikipedia

    en.wikipedia.org/wiki/Basal_ganglia

    Dysfunction of the basal ganglia circuitry can also lead to other disorders. [ 43 ] The following is a list of disorders, conditions, and symptoms that have been linked to the basal ganglia: [ citation needed ]

  5. Neuroferritinopathy - Wikipedia

    en.wikipedia.org/wiki/Neuroferritinopathy

    Neuroferritinopathy is a genetic neurodegenerative disorder characterized by the accumulation of iron in the basal ganglia, cerebellum, and motor cortex of the human brain. . Symptoms, which are extrapyramidal in nature, progress slowly and generally do not become apparent until adulthood

  6. Corticobasal degeneration - Wikipedia

    en.wikipedia.org/wiki/Corticobasal_degeneration

    Corticobasal degeneration (CBD) is a rare neurodegenerative disease involving the cerebral cortex and the basal ganglia. [1] CBD symptoms typically begin in people from 50 to 70 years of age, and typical survival before death is eight years.

  7. Primary familial brain calcification - Wikipedia

    en.wikipedia.org/wiki/Primary_familial_brain...

    Primary familial brain calcification [1] (PFBC), also known as familial idiopathic basal ganglia calcification (FIBGC) and Fahr's disease, [1] is a rare, [2] genetically dominant or recessive, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement.

  8. Athetosis - Wikipedia

    en.wikipedia.org/wiki/Athetosis

    Athetosis is a symptom primarily caused by the marbling, or degeneration of the basal ganglia. [citation needed] This degeneration is most commonly caused by complications at birth or by Huntington's disease, in addition to rare cases in which the damage may also arise later in life due to stroke or trauma.

  9. Hypokinesia - Wikipedia

    en.wikipedia.org/wiki/Hypokinesia

    Hypokinetic symptoms arise from damage to the basal ganglia, which plays a role in producing force and computing the effort necessary to make a movement. [17] Two possible neural pathways enable the basal ganglia to produce movement.