Consanguineous 3-methylcrotonyl-CoA carboxylase deficiency: early-onset necrotizing encephalopathy with lethal outcome.

Abstract

A patient with a severe neonatal variant of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency is reported. The first child of healthy consanguineous Turkish parents presented on the second day of life with dehydration, cyanosis, no sucking, generalized muscular hypotonia, encephalopathy, respiratory depression requiring mechanic ventilation, macrocephaly, severe acidosis and hypoglycaemia. Elevated C5-OH-carnitine in dried blood spot by tandem MS and elevated urinary excretion of 3-hydroxyisovaleric acid and 3-methylcrotonylglycine suggested MCC deficiency, confirmed by enzyme analysis in cultured fibroblasts. Cerebral ultrasonography and cranial CT findings revealed progressive changes such as disseminated encephalomalacia, cystic changes, ventricular dilatation and cerebral atrophy. Treatment with high-dose biotin and protein-restricted diet was ineffective and the patient died at the age of 33 days with progressive neurological deterioration. Mutation analysis revealed a homozygous mutation in the splice acceptor site of intron 15 in the MCC beta-subunit. Early-onset severe necrotizing encephalopathy should be included in the differential diagnosis of isolated MCC deficiency.

• Authors: T Baykal, G Huner Gokcay, Z Ince, M F Dantas, B Fowler, M R Baumgartner, F Demir, G Can, M Demirkol
• Journal: Journal of inherited metabolic disease (J Inherit Metab Dis) Vol. 28 Issue 2 Pg. 229-33 ( 2005) ISSN: 0141-8955 [Print] United States
• PMID: 15877210 (Publication Type: Case Reports, Journal Article)

Chemical References

• RNA Splice Sites
• Valerates
• beta-methylcrotonylglycine
• beta-hydroxyisovaleric acid
• Carbon-Carbon Ligases
• methylcrotonoyl-CoA carboxylase
• Glycine

Topics

• Carbon-Carbon Ligases (deficiency, genetics)
• Consanguinity
• Diagnosis, Differential
• Fatal Outcome
• Glycine (analogs & derivatives, urine)
• Humans
• Infant
• Infant, Newborn
• Leukoencephalitis, Acute Hemorrhagic (diagnosis, etiology)
• Male
• Metabolism, Inborn Errors (complications, diagnosis, genetics)
• Mutation
• RNA Splice Sites (genetics)
• Valerates (urine)