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1 Introduction Loeys–Dietz syndrome (LDS) is an autosomal dominant connective tissue disorder presenting with cardiovascular, skeletal, and craniofacial features. It has significant clinical overlap with other connective tissue disorders such as Marfan syndrome [MIM: 154700]. Overlapping features include thoracic aortic aneurysm and dissection (TAAD), pectus deformity, scoliosis, joint laxity, arachnodactyly, and talipes equinovarus.
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