1. A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: A case report with clinical and molecular review.
- Author
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Galvão de Oliveira M, Tengan C, Micheletti C, Ramos de Macedo P, Soares Pinho Cernach MC, Cavole TR, de França Basto M, Filho JS, Virmond LA, Milanezi F, Nakano V, Falconi A, and Perrone E
- Subjects
- Cardiomyopathy, Hypertrophic pathology, Cytochrome-c Oxidase Deficiency pathology, Heterozygote, Humans, Infant, Newborn, Male, Mitochondrial Encephalomyopathies pathology, Mutation, Phenotype, Cardiomyopathy, Hypertrophic genetics, Cytochrome-c Oxidase Deficiency genetics, Electron Transport Complex IV genetics, Mitochondrial Encephalomyopathies genetics
- Abstract
The cytochrome c-oxidase (COX) enzyme, also known as mitochondrial complex IV (MT-C4D), is a transmembrane protein complex found in mitochondria. COX deficiency is one of the most frequent causes of electron transport chain defects in humans. Therefore, high energy demand organs and tissues are affected in patients with mutations in the COX15 gene, with variable phenotypic expressiveness. We describe the case of a male newborn with hypertrophic cardiomyopathy and serum and cerebrospinal fluid hyperlacticaemia, whose exome sequencing revealed two variants in a compound heterozygous state: c.232G > A; p.(Gly78Arg), classified as likely pathogenic, and c.452C > G; p.(Ser151Ter), as pathogenic; the former never previously described in the literature., (Copyright © 2021 Elsevier Masson SAS. All rights reserved.)
- Published
- 2021
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