A TNNT2 variant in a sporadic case of dilated cardiomyopathy: a case report and review.

Purpose: This study aims to characterize the clinical and genetic features of a sporadic case of dilated cardiomyopathy (DCM) associated with a TNNT2 variant and to review the variant spectrum of the TNNT2 gene in the Chinese DCM population. Patients and methods: A 41-year-old male proband diagnosed with DCM underwent comprehensive clinical evaluation. Whole-exome sequencing (WES) was performed on the proband to identify potential causative variants. Subsequently, Sanger sequencing was used to specifically validate the candidate TNNT2 variant in the proband and all available family members. Bioinformatic tools were employed to predict the pathogenicity of the identified variant, which was interpreted according to the American College of Medical Genetics and Genomics (ACMG) guidelines. A literature review of TNNT2 variants in Chinese DCM patients was conducted. Results: Clinical assessment revealed left ventricular dilation and systolic dysfunction in the proband. Genetic analysis identified a heterozygous missense variant in the TNNT2 gene (c.311G > A, p.Arg104His). Bioinformatic predictions consistently supported its deleterious effect and high conservation. The variant was not found in the available family members. Considering the maternal sudden death history, it is likely to be Conclusion: This study provides a detailed clinical characterization of the TNNT2 c.311G > A (p.Arg104His) variant in a Chinese patient with sporadic DCM, contributing to the understanding of its phenotypic spectrum. The review provides an overview of the TNNT2 variant spectrum in the Chinese DCM population.