Credite: dokteranakku.net |
Chorea (or choreia, occasionally) is an abnormal involuntary
movement disorder, one of a group of neurological disorders called dyskinesias.
The term chorea is derived from the Greek word χορεία (=dance; see choreia), as
the quick movements of the feet or hands are comparable to dancing.
The term hemichorea refers to chorea of one side of the
body, such as chorea of one arm but not both (analogous to hemiballismus).
Presentation
Chorea is characterized by brief, semi-directed, irregular
movements that are not repetitive or rhythmic, but appear to flow from one
muscle to the next.
These 'dance-like' movements of chorea often occur with
athetosis, which adds twisting and writhing movements. Walking may become
difficult, and include
odd postures and leg movements.
Unlike ataxia, which affects the quality of voluntary
movements, or Parkinsonism, which is a hindrance of voluntary movements, the
movements of chorea and ballism occur on their own, without conscious effort.
Thus, chorea is said to be a hyperkinetic movement disorder.
When chorea is serious, slight movements will become
thrashing motions; this form of severe chorea is referred to as ballism or
ballismus.
Causes
Huntington’s disease
Huntington's disease is a neurodegenerative disease and the
commonest inherited cause of chorea. The condition was formerly called
Huntington's chorea but was renamed because of the important non-choreic
features including cognitive decline and behavioural change.
Other genetic causes
Other genetic causes of chorea are rare. They include the
classical Huntington's disease 'mimic' or phenocopy syndromes, called
Huntington's disease-like syndrome types 1, 2 and 3; inherited prion disease,
the spinocerebellar ataxias type 1, 3 and 17, neuroacanthocytosis,
dentatorubral-pallidoluysian atrophy (DRPLA), brain iron accumulation
disorders, Wilson's disease, benign hereditary chorea, Friedreich's ataxia,
mitochondrial disease and Rett syndrome.
Acquired causes
The commonest acquired causes of chorea are cerebrovascular
disease and, in the developing world, HIV infection - usually through its
association with cryptococcal disease.
Sydenham's chorea occurs as a complication of streptococcal
infection. Twenty percent (20%) of children and adolescents with rheumatic
fever develop Sydenham's chorea as a complication. It is increasingly rare,
which may be partially due to penicillin, improved social conditions, and/or a
natural reduction in the bacteria ( Streptococcus ) it has stemmed from.
Psychological symptoms may precede or accompany this acquired chorea and may be
relapsing and remitting. The broader spectrum of paediatric autoimmune
neuropsychiatric disorders associated with streptococcal infection can cause
chorea and are collectively referred to as PANDAS.
Chorea gravidarum refers to choreic symptoms that occur
during a women’s pregnancy. If left untreated, the disease resolves in 30% of
patients before delivery but, in the other 70%, it persists. The symptoms then
progressively disappear in the next few days following the delivery.
Chorea may also be caused by drugs (commonly levodopa,
anti-convulsants and anti-psychotics).
Other acquired causes include systemic lupus erythematosus,
antiphospholipid syndrome, thyrotoxicosis, polycythaemia rubra vera, transmissible spongiform encephalopathies and coeliac disease.
Form
|
Treatment
|
Huntington's-related
|
A common treatment is dopaminergic antagonists, although treatment
is largely supportive. Tetrabenazine is
the only FDA approved drug for the treatment of Huntington's Disease related
chorea.
|
Sydenham's chorea
|
Haloperidol, carbamazepine and valproic acid. Usually
involves antibiotic drugs to treat the infection, followed
by drug therapy to prevent recurrence.
|
Chorea gravidarum
|
haloperidol, chlorpromazine alone
or in combination with diazepam, also pimozide can
also be used.
|
Wilson's disease
|
|
Drug-induced chorea
|
Adjusting medication dosages.
|
Metabolic and endocrine-related choreas
|
Treated according to their causes.
|
No comments:
Post a Comment