Neurologic deterioration in a child with Wilson's disease on penicillamine therapy.
Article
Dans Anglais
| IMSEAR
| ID: sea-65618
ABSTRACT
Penicillamine is the standard therapy for Wilson's disease in children. We report an 8-year-old-girl with liver disease due to Wilson's disease who developed extrapyramidal symptoms following administration of penicillamine. Symptoms resolved within 20 hours of stopping the drug but recurred within 24 hours when gradually increasing small doses were recommenced.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Pénicillamine
/
Syndrome
/
Femelle
/
Humains
/
Chélateurs
/
Enfant
/
Maladies neurodégénératives
/
Relation dose-effet des médicaments
/
Dégénérescence hépatolenticulaire
langue:
Anglais
Année:
2003
Type:
Article
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