Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency

Anne Davidson-Mundt; Anthony S. Luder; Carol L. Greene

doi:10.1016/s0022-3476(05)80918-7

Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency

Anne Davidson-Mundt, Anthony S. Luder, Carol L. Greene

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

Six infants and children with medium-chain acyl-coenzyme A dehydrogenase deficiency were found to have hyperuricemia during an acute episode. Hyperuricemia may be a clue to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.

Original language	English
Pages (from-to)	444-446
Number of pages	3
Journal	Journal of Pediatrics
Volume	120
Issue number	3
DOIs	https://doi.org/10.1016/s0022-3476(05)80918-7
State	Published - Mar 1992
Externally published	Yes

Bibliographical note

Funding Information:
Supported in part by Special Projects of National and Regional Significance grant No. MCJ-000252. Bureau of Maternal and Child Health and Resources Development, U.S. Department of Health and Human Services, and by General Clinical Research Centers Program grant No. RR-69, National Institutes of Health. Submitted for publication Dec. 31. 1990: accepted Oct. 3. 1991. Reprint requests: A. Davidson-Mundt. RN. MS, Children's Hospital, 1056 E. 19th Ave., Box B-153, Denver, CO 80218. 9/22/34171 Increased serum uric acid levels have been rePorted in disorders of fatty acid metabolism, 3 but the significance of hyperuricemia in the differential diagnosis of encephalopathy in children has not been emphasized.

Funding

Supported in part by Special Projects of National and Regional Significance grant No. MCJ-000252. Bureau of Maternal and Child Health and Resources Development, U.S. Department of Health and Human Services, and by General Clinical Research Centers Program grant No. RR-69, National Institutes of Health. Submitted for publication Dec. 31. 1990: accepted Oct. 3. 1991. Reprint requests: A. Davidson-Mundt. RN. MS, Children's Hospital, 1056 E. 19th Ave., Box B-153, Denver, CO 80218. 9/22/34171 Increased serum uric acid levels have been rePorted in disorders of fatty acid metabolism, 3 but the significance of hyperuricemia in the differential diagnosis of encephalopathy in children has not been emphasized.

Funders	Funder number
Bureau of Maternal and Child Health and Resources Development
General Clinical Research Centers Program	RR-69
Special Projects of National and Regional Significance	MCJ-000252
National Institutes of Health
U.S. Department of Health and Human Services

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title = "Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency",

abstract = "Six infants and children with medium-chain acyl-coenzyme A dehydrogenase deficiency were found to have hyperuricemia during an acute episode. Hyperuricemia may be a clue to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.",

author = "Anne Davidson-Mundt and Luder, \{Anthony S.\} and Greene, \{Carol L.\}",

note = "Funding Information: Supported in part by Special Projects of National and Regional Significance grant No. MCJ-000252. Bureau of Maternal and Child Health and Resources Development, U.S. Department of Health and Human Services, and by General Clinical Research Centers Program grant No. RR-69, National Institutes of Health. Submitted for publication Dec. 31. 1990: accepted Oct. 3. 1991. Reprint requests: A. Davidson-Mundt. RN. MS, Children's Hospital, 1056 E. 19th Ave., Box B-153, Denver, CO 80218. 9/22/34171 Increased serum uric acid levels have been rePorted in disorders of fatty acid metabolism, 3 but the significance of hyperuricemia in the differential diagnosis of encephalopathy in children has not been emphasized.",

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Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency

Abstract

Bibliographical note

Funding

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