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Clin Genet ; 91(1): 46-53, 2017 01.
Article in English | MEDLINE | ID: mdl-27256614

ABSTRACT

We report clinical and biochemical finding from three unrelated patients presenting ONCE (Optic Neuropathy, Cardiomyopathy and Encephalopathy with lactic acidosis and combined oxidative phosphorylation deficiency) syndrome. Whole-exome sequencing (WES) of the three patients and the healthy sister of one of them was used to identify the carry gene. Clinical and biochemical findings were used to filter variants, and molecular, in silico and genetic studies were performed to characterize the candidate variants. Mitochondrial DNA (mtDNA) defects involving mutations, deletions or depletion were discarded, whereas WES uncovered a double homozygous mutation in the MTO1 gene (NM_001123226:c.1510C>T, p.R504C, and c.1669G>A, p.V557M) in two of the patients and the homozygous mutation p.R504C in the other. Therefore, our data confirm p.R504C as pathogenic mutation responsible of ONCE syndrome, and p.V557M as a rare polymorphic variant.


Subject(s)
Abnormalities, Multiple/genetics , Carrier Proteins/genetics , Genetic Predisposition to Disease/genetics , Mutation, Missense , Polymorphism, Single Nucleotide , Abnormalities, Multiple/pathology , Acidosis, Lactic , Adolescent , Amino Acid Sequence , Brain Diseases , Cardiomyopathies , Exome/genetics , Family Health , Female , Homozygote , Humans , Male , Mitochondrial Diseases , Optic Nerve Diseases , Pedigree , RNA-Binding Proteins , Sequence Analysis, DNA , Sequence Homology, Amino Acid , Syndrome , Young Adult
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