N J Med. 1992 May;89(5):385-92.

Medium chain acyl-coenzyme A dehydrogenase deficiency and SIDS.

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Division of Neonatology, St. Peter's Medical Center, UMDNJ-Robert Wood Johnson Medical School, New Brunswick 08903.

Abstract

Medium chain acyl-coenzyme A dehydrogenase deficiency (MCADD) is a potentially fatal genetic defect in fatty acid metabolism and may account for a proportion of all deaths initially attributed to sudden infant death syndrome (SIDS). Effective therapy and prevention are available.

PMID:: 1635678; [PubMed - indexed for MEDLINE]

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Review Medium chain acyl-coenzyme A dehydrogenase deficiency. [N J Med. 1992]
Review Medium chain acyl-coenzyme A dehydrogenase deficiency.
Bennett MJ, Hale DE. N J Med. 1992 Sep; 89(9):675-8.
Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome. [J Pediatr. 1993]
Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome.
Arens R, Gozal D, Jain K, Muscati S, Heuser ET, Williams JC, Keens TG, Ward SL. J Pediatr. 1993 May; 122(5 Pt 1):715-8.
Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death. [N Engl J Med. 1991]
Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death.
Ding JH, Roe CR, Iafolla AK, Chen YT. N Engl J Med. 1991 Jul 4; 325(1):61-2.
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency. [Pediatrics. 1986]
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
Duran M, Hofkamp M, Rhead WJ, Saudubray JM, Wadman SK. Pediatrics. 1986 Dec; 78(6):1052-7.
Review A fatal neonatal case of medium-chain acyl-coenzyme A dehydrogenase deficiency with homozygous A-->G985 transition. [J Pediatr. 1992]
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Leung KC, Hammond JW, Chabra S, Carpenter KH, Potter M, Wilcken B. J Pediatr. 1992 Dec; 121(6):965-8.

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