A deleterious MYH11 mutation causing familial thoracic aortic dissection

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Abstract

The L1264P and R1275L heterozygous mutations of the myosin heavy chain 11 (MYH11) gene, which are on the same allele, have been reported to cause thoracic aortic aneurysms and/or dissections (TAAD) complicated with patent ductus arteriosus (PDA); however, their contributions to the pathogenesis of TAAD/PDA have not been elucidated. Here we report the first familial case of TAAD with only a MYH11 L1264P mutation, in which PDA was not observed, indicating that L1264P, not R1275L, is responsible for TAAD formation.

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Takeda, N., Morita, H., Fujita, D., Inuzuka, R., Taniguchi, Y., Nawata, K., & Komuro, I. (2015). A deleterious MYH11 mutation causing familial thoracic aortic dissection. Human Genome Variation, 2(1). https://doi.org/10.1038/HGV.2015.28

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