207 top medical experts on Dihydropyrimidine Dehydrogenase Deficiency across 19 countries and 11 U.S. states, including 36 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Dihydropyrimidine Dehydrogenase Deficiency: An autosomal recessive disorder affecting dihydropyrimidine dehydrogenase and causing familial pyrimidinemia. It is characterized by thymine-uraciluria in homozygous deficient patients. Even a partial deficiency in the enzyme leaves individuals at risk for developing severe 5-fluorouracil-associated toxicity.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Inborn Errors Purine-Pyrimidine Metabolism (580).
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