Key result
Exome sequencing links TANGO2 variants to an expanded clinical phenotype of primarily neurological presentations.
Why the study?
The clinical phenotype and spectrum of pathogenic variants in TANGO2-related disorders have not been fully characterized since initial descriptions.
Case Report (n=14)
TANGO2-related disorders have a more diverse clinical presentation than previously anticipated, highlighting the utility of routine exome sequencing data reanalysis.
May warrant TANGO2 consideration in unexplained neurology; extends phenotype but remains hypothesis-generating.
PURPOSE: TANGO2-related disorders were first described in 2016 and prior to this publication, only 15 individuals with TANGO2-related disorder were described in the literature. Primary features include metabolic crisis with rhabdomyolysis, encephalopathy, intellectual disability, seizures, and cardiac arrhythmias. We assess whether genotype and phenotype of TANGO2-related disorder has expanded since the initial discovery and determine the efficacy of exome sequencing (ES) as a diagnostic tool for detecting variants. METHODS: We present a series of 14 individuals from 11 unrelated families with complex medical and developmental histories, in whom ES or microarray identified compound heterozygous or homozygous variants in TANGO2. RESULTS: The initial presentation of patients with TANGO2-related disorders can be variable, including primarily neurological presentations. We expand the phenotype and genotype for TANGO2, highlighting the variability of the disorder. CONCLUSION: TANGO2-related disorders can have a more diverse clinical presentation than previously anticipated. We illustrate the utility of routine ES data reanalysis whereby discovery of novel disease genes can lead to a diagnosis in previously unsolved cases and the need for additional copy-number variation analysis when ES is performed.
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Dines et al. (2018) conducted a case report in TANGO2-related disorders (n=14). Exome sequencing (ES) or microarray was evaluated on Phenotypic and genotypic expansion of TANGO2-related disorders. Exome sequencing and microarray identified TANGO2 variants in 14 individuals, expanding the known clinical phenotype to include primarily neurological presentations.
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