Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected association.

Abstract

MC, female, is the third child of a nonconsanguineous Portuguese couple, born after an uneventful pregnancy and delivery. A positive family history of ornithine transcarbamylase deficiency, associated with the IVS8+1 G>A mutation in the ornithine transcarbamylase gene, prompted prenatal diagnosis with identification of the same mutation in the proband. During an episode of Klebsiella pneumoniae sepsis at 1.5 months of age, lactic acidosis and moderate hyperammonemia were noticed. After a short asymptomatic period, progressive neurologic symptoms, with normal ammonemia, persistent hyperlactacidemia, and typical lesions in brain computed tomography (CT) scan led to a diagnosis of Leigh syndrome. Mitochondrial respiratory chain complex V was reduced in the liver. The mtDNA 8993T>G mutation was identified in the liver, muscle, and blood (82%-87% heteroplasmy). She died at 6 months of age. This case represents a benign phenotype of ornithine transcarbamylase deficiency, associated with a severe mitochondrial respiratory chain disorder due to an mtDNA pathogenic mutation.

• Authors: Margarida Henriques, Luísa Diogo, Paula Garcia, João Pratas, Marta Simões, Manuela Grazina
• Journal: Journal of child neurology (J Child Neurol) Vol. 27 Issue 8 Pg. 1059-61 (Aug 2012) ISSN: 1708-8283 [Electronic] United States
• PMID: 22241703 (Publication Type: Journal Article)

Chemical References

• DNA, Mitochondrial

Topics

• Child, Preschool
• DNA, Mitochondrial (genetics)
• Female
• Humans
• Infant
• Leigh Disease (complications, genetics)
• Muscles (pathology)
• Mutation (genetics)
• Ornithine Carbamoyltransferase Deficiency Disease (complications, genetics)