Dihydropyrimidine dehydrogenase deficiency in a Hutterite newborn

Adv Exp Med Biol. 1991:309B:311-4. doi: 10.1007/978-1-4615-7703-4_69.

Authors

K J Adolph¹, E Fung, D R McLeod, K Morgan, F F Snyder

Affiliation

¹ Department of Paediatrics, University of Calgary, Alberta, Canada.

PMID: 1781388
DOI: 10.1007/978-1-4615-7703-4_69

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Alberta
Consanguinity
Dihydrouracil Dehydrogenase (NADP)
Ethnicity
Humans
Infant, Newborn
Male
Oxidoreductases / deficiency*
Purine-Pyrimidine Metabolism, Inborn Errors / enzymology*
Purine-Pyrimidine Metabolism, Inborn Errors / genetics
Purine-Pyrimidine Metabolism, Inborn Errors / urine
T-Lymphocytes / enzymology
Thymine / urine
Uracil / urine

Substances

Uracil
Oxidoreductases
Dihydrouracil Dehydrogenase (NADP)
Thymine