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A new case of dihydropyrimidine dehydrogenase deficiency
M Brockstedt1, C Jakobs, L M Smit
1Dept. of Pediatrics, Free University Hospital, Amsterdam, The Netherlands.
Journal of Inherited Metabolic Disease
|January 1, 1990
Abstract:
We present the clinical and biochemical features of a boy with dihydropyrimidine dehydrogenase deficiency, which seem to underline a disease entity of developmental retardation, epilepsy and muscular hypertonia.
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