PRENATAL DIAGNOSIS OF MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY IN FAMILY WITH SUDDEN INFANT DEATH
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndrome;Roe;J Pediatr,1986
2. Sudden child death and "healthy" affected family members with medium-chain acyl-CoA dehydrogenase deficiency;Duran;Pediatrics,1986
3. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: Studies in cultured skm fibroblasts and peripheral mononuclear leukocytes;Coates;Pediatr Res,1985
4. Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts;Frerman;Biochem Med,1985
5. Deficiency of medium-chain acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome;Howat;Br Med J,1984
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2. Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counseling;Journal of Genetic Counseling;1993-03
3. Medium chain acyl-CoA dehydrogenase deficiency.;Archives of Disease in Childhood;1992-01-01
4. Prenatal exclusion of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency by direct detection of the mutation with PCR;Prenatal Diagnosis;1992-01
5. Topical Review Article: Organic Acidurias: A Review Part 2;Journal of Child Neurology;1991-10
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