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  2. MASA syndrome - Wikipedia

    en.wikipedia.org/wiki/MASA_syndrome

    The first case of the MASA Syndrome was found in a boy in Asia. The patient was a 10-year-old boy with symptoms like, mild mental retardation, bilateral adducted thumbs and corpus callosum hypoplasia. [15] His family did not have any history with MASA syndrome. There is not just one specific doctor or scientist for this disorder.

  3. Cerebral arteriovenous malformation - Wikipedia

    en.wikipedia.org/wiki/Cerebral_arteriovenous...

    Symptoms due to bleeding include loss of consciousness, sudden and severe headache, nausea, vomiting, incontinence, and blurred vision, amongst others. [4] Impairments caused by local brain-tissue damage on the bleed site are also possible, including seizure, one-sided weakness ( hemiparesis ), a loss of touch sensation on one side of the body ...

  4. Inflammatory demyelinating diseases of the central nervous ...

    en.wikipedia.org/wiki/Inflammatory_demyelinating...

    It has also been proposed that always exists a subclinical phase in the beginning of every MS case, during which the permeability of the BBB can be used for diagnosis [142] It is also under investigation whether MS has a prodrome, i.e., a preliminary stage in which the disease exists with non-specific symptoms. Some reports point to a prodrome ...

  5. Middle cerebral artery syndrome - Wikipedia

    en.wikipedia.org/wiki/Middle_cerebral_artery...

    Middle cerebral artery syndrome is a condition whereby the blood supply from the middle cerebral artery (MCA) is restricted, leading to a reduction of the function of the portions of the brain supplied by that vessel: the lateral aspects of frontal, temporal and parietal lobes, the corona radiata, globus pallidus, caudate and putamen.

  6. Postperfusion syndrome - Wikipedia

    en.wikipedia.org/wiki/Postperfusion_syndrome

    Symptoms of postperfusion syndrome are subtle and include defects associated with attention, concentration, short-term memory, fine motor function, and speed of mental and motor responses. [1] Studies have shown a high incidence of neurocognitive deficit soon after surgery, but the deficits are often transient with no permanent neurological ...

  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. Cerebellar degeneration - Wikipedia

    en.wikipedia.org/wiki/Cerebellar_degeneration

    More specifically, the neurological diseases that can cause cerebellar degeneration include: [11] Diagram of two different nerve cells. The diagram on the left shows a nerve cell that is healthy and normally-functioning. The diagram on the right shows a nerve cell with a damaged myelin sheath, being the cause of multiple sclerosis.

  9. Tardive dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Tardive_dyskinesia

    Often the symptoms of tardive dyskinesia are not apparent until the individual comes off of the antipsychotic drugs; however, when tardive dyskinesia worsens, the signs become visible. [24] Other dopamine antagonists and antiemetics can cause tardive dyskinesia, such as metoclopramide and promethazine, used to treat gastrointestinal disorders.