juvenile chorea - translation to αραβικά
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juvenile chorea - translation to αραβικά

HUMAN DISEASE
Choreoacanthocytosis; Acanthocytosis chorea; Chorea acanthocytosis

juvenile chorea      
‎ رَقَصٌ يَفَعِيّ‎
rheumatic chorea         
  • Erythema marginatum
  • Penicillin
DISORDER CHARACTERIZED BY RAPID, UNCOORDINATED JERKING MOVEMENTS PRIMARILY AFFECTING THE FACE, HANDS AND FEET
Sydenhams Chorea; Sydenham's Chorea; Rheumatic Chorea; Rheumatic chorea; Sydenham Chorea; Sydenham chorea; Chorea minor; Chorea St. Viti; Sydenham’s disease; Sydenham’s syndrome; Sydenham's Chorea or St Vitus Dance; Milk sign; Chorea van Sydenham
‎ رَقَصٌ روماتزميّ‎
CHOREA         
MOVEMENT DISEASE CHARACTERIZED BY BRIEF, SEMI-DIRECTED, IRREGULAR MOVEMENTS THAT NOT REPETITIVE OR RHYTHMIC, BUT APPEAR TO FLOW FROM ONE MUSCLE TO THE NEXT
Chorea sancti viti; Choreatic disorders; El Mal de San Vitus; El Mal de San Vito; Hemichorea; Choreiform movement; Chorea (disease); Wǔdǎozhèng; Choreia (disease); Chorea (disorder); Canine chorea

ألاسم

الرقاص مرض عصبي

Ορισμός

Sydenham's chorea
¦ noun a form of chorea chiefly affecting children, associated with rheumatic fever.
Origin
C19: named after the 17th-cent. English physician Thomas Sydenham.

Βικιπαίδεια

Chorea-acanthocytosis

Chorea-acanthocytosis (ChAc, also called choreoacanthocytosis) is a rare hereditary disease caused by a mutation in a gene that directs structural proteins in red blood cells. It belongs to a group of four diseases characterized under the name neuroacanthocytosis. When a patient's blood is viewed under a microscope, some of the red blood cells appear thorny. These thorny cells are called acanthocytes.

Other effects of the disease may include epilepsy, behaviour changes, muscle degeneration, and neuronal degradation similar to Huntington's disease. The average age of onset of symptoms is 35 years. The disease is incurable and inevitably leads to premature death.

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.

This disease is also characterized by the presence of a few different movement disorders including chorea, dystonia etc.

Chorea-acanthocytosis is considered an autosomal recessive disorder, although a few cases with autosomal dominant inheritance have been noted.