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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007
See this aricle in Pubmed

Article Abstract
The clinical presentations were as follows: hepatic, 42 (14.9%); hepato-neurologic, 10 (3.5%); neurologic, 195 (69.1%); pure psychiatric, 7 (2.4%); osseomuscular, 6 (2.1%); and presymptomatic, 15 (5.3%). Mean age was 15.9 years. Presymptomatic patients and those with the hepatic form of WD were younger and patients with osseomuscular and psychiatric forms were older than neurologic patients. The mean duration of illness at the time of diagnosis was 28 months. Predominant neurologic features were as follows: parkinsonism, 62.3%; dystonia, 35.4%; cerebellar, 28%; pyramidal signs, 16%; chorea, 9%; athetosis, 2.2%; myoclonus, 3.4%; and behavioral abnormalities, 16%. Kayser-Fleischer (KF) rings were seen as follows: neurologic patients, 100%; hepatic patients, 86%; and presymptomatic patients, 59%. Positive family history was noted in 47% and consanguinity in 54%.
 
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asymptomatic
ceruloplasmin,serum
chorea
choreoathetosis
consanguinity
copper metabolism,abnormal
delay in diagnosis
dystonia
familial
hepatic failure
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
Kayser-Fleischer ring
liver disease
mortality
movement disorder
MRI
MRI,abnormal
myoclonus
Parkinsonism syndrome
penicillamine
prognosis
psychiatric problems in neurologic disorders
review article
treatment of neurologic disorder

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