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Abstract
A 28-year-old Japanese man with recurrent crises of excruciating pain in the limbs
and lack of sweating since childhood was found to have angiokeratomata on the scrotum.
Thin layer chromatographic studies of the urinary sediment disclosed an abnormal accumulation
of ceramide trihexoside and confirmed the diagnosis of Fabry's disease. The family
history revealed evidence of renal disease in the patient's mother. The painful crises
were treated successfully with carbamazepine in a daily dosage of 200 mg. The pharmacological
actions of carbamazepine in suppressing various epileptic or painful conditions are
reviewed.
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Article info
Publication history
Received:
August 1,
1972
Identification
Copyright
© 1973 Published by Elsevier Inc.