Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs
- PMID: 7128647
- DOI: 10.1007/BF00442517
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs
Abstract
Two Vietnamese siblings with an isolated deficiency of 3-methylcrotonyl coenzyme A carboxylase in leucocytes and cultured fibroblasts are described. Both children excreted massive amounts of 3-methylcrotonylglycine and 3-hydroxyisovaleric acid. There was no in vivo or in vitro biochemical response to biotin. Apart from an attack of vomiting leading to subcoma in the elder sib four weeks after arrival in the Netherlands, the children were in good health. There were no signs of delayed mental development.
Similar articles
-
A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.Clin Chim Acta. 1980 Jan 15;100(2):183-6. doi: 10.1016/0009-8981(80)90081-9. Clin Chim Acta. 1980. PMID: 6766095
-
Reassessment of biotin-responsiveness in "unresponsive" propionyl CoA carboxylase deficiency.J Pediatr. 1980 Dec;97(6):964-6. doi: 10.1016/s0022-3476(80)80437-9. J Pediatr. 1980. PMID: 7441430 No abstract available.
-
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency: long-term outcome in a case with neonatal onset.Eur J Pediatr. 1996 Jul;155(7):568-72. doi: 10.1007/BF01957906. Eur J Pediatr. 1996. PMID: 8831079
-
Biotin in clinical medicine--a review.Am J Clin Nutr. 1981 Sep;34(9):1967-74. doi: 10.1093/ajcn/34.9.1967. Am J Clin Nutr. 1981. PMID: 6116428 Review.
-
Molecular mechanism of dominant expression in 3-methylcrotonyl-CoA carboxylase deficiency.J Inherit Metab Dis. 2005;28(3):301-9. doi: 10.1007/s10545-005-7054-3. J Inherit Metab Dis. 2005. PMID: 15868465 Review.
Cited by
-
Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblasts.Am J Hum Genet. 1984 Jul;36(4):791-801. Am J Hum Genet. 1984. PMID: 6475954 Free PMC article.
-
3-Methylglutaconic and 3-methylglutaric aciduria in a patient with suspected 3-methylglutaconyl-CoA hydratase deficiency.Eur J Pediatr. 1985 Mar;143(4):301-3. doi: 10.1007/BF00442306. Eur J Pediatr. 1985. PMID: 2580710
-
Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD.Genet Med. 2015 Aug;17(8):660-7. doi: 10.1038/gim.2014.157. Epub 2014 Nov 6. Genet Med. 2015. PMID: 25356967 Free PMC article.
-
Isolated biotin-resistant 3-methylcrotonyl CoA carboxylase deficiency presenting with life-threatening hypoglycaemia.J Inherit Metab Dis. 1984;7(4):182. doi: 10.1007/BF01805608. J Inherit Metab Dis. 1984. PMID: 6441868 No abstract available.
-
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness.J Inherit Metab Dis. 1989;12(3):339-40. doi: 10.1007/BF01799234. J Inherit Metab Dis. 1989. PMID: 2515383 No abstract available.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical