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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. Basal ganglia - Wikipedia

    en.wikipedia.org/wiki/Basal_ganglia

    The basal ganglia (BG) or basal nuclei ... The following is a list of disorders, conditions, and symptoms that have been linked to the basal ganglia: [citation needed ...

  4. 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.

  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. Doctors Say This Nighttime Behavior Can Be A Sign Of Dementia

    www.aol.com/doctors-nighttime-behavior-sign...

    Also known as “sundowner’s syndrome,” sundowning is a set of symptoms or behaviors that can be seen in some people with Alzheimer’s disease and dementia, according to the Alzheimer’s ...

  9. Hemiballismus - Wikipedia

    en.wikipedia.org/wiki/Hemiballismus

    Hemiballismus or hemiballism is a basal ganglia syndrome resulting from damage to the subthalamic nucleus in the basal ganglia. [1] It is a rare hyperkinetic movement disorder, [2] that is characterized by pronounced involuntary limb movements [1] [3] on one side of the body [4] and can cause significant disability. [5]