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  2. Chorea - Wikipedia

    en.wikipedia.org/wiki/Chorea

    Chorea, or (rarely) choreia, (/ k ə ˈ r i ə /) is an abnormal involuntary movement disorder, characterized by quick movements of the hands or feet. It is one of a group of neurological disorders called dyskinesias .

  3. Choreoathetosis - Wikipedia

    en.wikipedia.org/wiki/Choreoathetosis

    Choreoathetosis is the occurrence of involuntary movements in a combination of chorea (irregular migrating contractions) and athetosis (twisting and writhing).. It is caused by many different diseases and agents.

  4. Benign hereditary chorea - Wikipedia

    en.wikipedia.org/wiki/Benign_hereditary_chorea

    Benign Hereditary Chorea is characterized by early onset of an abnormal gait, speech articulation difficulties, anxiety, and chorea. [5] The clinical spectrum of symptoms resulting from BHC is vast, manifesting as thyroid agenesis to dysarthria to distress syndrome. As a result, genetic testing is the only way to confirm the syndrome. [2]

  5. Huntington's disease - Wikipedia

    en.wikipedia.org/wiki/Huntington's_disease

    Huntington's disease (HD), also known as Huntington's chorea, is an incurable neurodegenerative disease [7] that is mostly inherited. [8] The earliest symptoms are often subtle problems with mood or mental/psychiatric abilities.

  6. 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 ...

  7. Paroxysmal kinesigenic dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Paroxysmal_kinesigenic...

    Paroxysmal kinesigenic dyskinesias are often inherited in an autosomal dominant fashion and several genes have now been identified where mutations can cause this disease. . The genes typically code for proteins known to be involved in synaptic transmission, ion channels or ion transporters.

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