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Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population.
- Source :
-
American journal of medical genetics. Part A [Am J Med Genet A] 2008 Mar 01; Vol. 146A (5), pp. 610-9. - Publication Year :
- 2008
-
Abstract
- Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is one of the most common fatty acid oxidation disorders. A subpopulation of children with MCADD present with metabolic crisis induced by fasting or illness, become lethargic, and can experience seizures or coma, culminating in a 20% mortality rate during the first episode. The frequency of these metabolic crises can be reduced with early diagnosis and treatment. The prevalence of MCADD in the United States is estimated to be 1 per 15,000 with p.K304E (c.985A > G) accounting for 90% of mutant alleles. In an 18-month period after initiating screening, the New York State Newborn Screening Mass Spectrometry Laboratory screened 385,893 newborns and referred 511 samples with elevated (>or=0.3 micromol/L) octanoylcarnitine (C8) levels for molecular testing. Of these referrals, six p.K304E homozygotes and 154 heterozygotes were identified. Twenty infants were biochemically confirmed with MCADD, per report from the child's pediatrician and/or treatment center. In these 20 cases, p.K304E accounted for only 47.5% of the mutant alleles. Further testing showed a second variant, p.Y42H, accounted for 7.5% of mutant alleles while the remaining 45% were unknown. Samples from all diagnosed non-p.K304E homozygous infants, and samples with C8 levels >or=1.0 micromol/L were sequenced (n = 16). Six novel and seven previously reported mutations were detected. These results suggest that p.K304E has a far lower representation in New York newborns with MCADD than current literature estimates and its full mutational spectrum is still unknown.<br /> ((c) 2008 Wiley-Liss, Inc.)
- Subjects :
- Base Sequence
Deficiency Diseases diagnosis
Deficiency Diseases epidemiology
Genetic Testing
Humans
Infant, Newborn
Molecular Sequence Data
Neonatal Screening
New York epidemiology
Population
Sequence Analysis, DNA
United States
Acyl-CoA Dehydrogenase deficiency
Acyl-CoA Dehydrogenase genetics
Point Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1552-4833
- Volume :
- 146A
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics. Part A
- Publication Type :
- Academic Journal
- Accession number :
- 18241067
- Full Text :
- https://doi.org/10.1002/ajmg.a.32192