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  2. Chorea gravidarum - Wikipedia

    en.wikipedia.org/wiki/Chorea_gravidarum

    Several pathogenetic mechanisms for chorea gravidarum have been offered, but none have been proven. History of either rheumatic fever or chorea is suspected: [2] [3] the suggestion is that estrogens and progesterone may sensitize dopamine receptors (presumably at a striatal level) and induce chorea in individuals who are vulnerable to this complication by virtue of preexisting pathology in the ...

  3. Chorea-acanthocytosis - Wikipedia

    en.wikipedia.org/wiki/Chorea-acanthocytosis

    Chorea-acanthocytosis is a very complex autosomal recessive adult-onset neurodegenerative disorder. It often shows itself as a mixed movement disorder, in which chorea, tics, dystonia and even parkinsonism may appear as a symptom. [3]

  4. Basal ganglia disease - Wikipedia

    en.wikipedia.org/wiki/Basal_ganglia_disease

    Huntington's disease is a hereditary disease that causes defects in behavior, cognition, and uncontrolled rapid, jerky movements. [1] Huntington's disease stems from a defect that consists of an expanded CAG repeat in the huntingtin gene (HTT) located on the short arm p of chromosome 4. [7]

  5. Benign hereditary chorea - Wikipedia

    en.wikipedia.org/wiki/Benign_hereditary_chorea

    Benign hereditary chorea (BHC), also known as benign familial chorea, is a rare autosomal dominant neurogenetic syndrome. It typically presents itself in childhood with isolated chorea , with average to below average intelligence.

  6. Neuroacanthocytosis - Wikipedia

    en.wikipedia.org/wiki/Neuroacanthocytosis

    Neuroacanthocytosis is a label applied to several genetic neurological conditions in which the blood contains misshapen, spiculated red blood cells called acanthocytes.. The 'core' neuroacanthocytosis syndromes, in which acanthocytes are a typical feature, are chorea acanthocytosis and McLeod syndrome.

  7. Thirteen (House) - Wikipedia

    en.wikipedia.org/wiki/Thirteen_(House)

    Thirteen has a 50/50 chance of having inherited Huntington's disease from her mother, but she initially refuses to be tested for it as not knowing allows her to live with hope. In the fourth-season finale, Thirteen takes the test and is diagnosed as having the mutated Huntington gene. [4]