Thoracic Outlet Syndrome: A Significant Family Genetic Phenotypic Presentation

Abstrakt

We report on a very rare case of diagnosis and successful surgical treatment of three young family members with a four-fold presentation of thoracic outlet syndrome. In the relevant family case, we are considering and discussing the population incidence, a possible HOX genes disorder, and a significant phenotypic presentation.

Klíčová slova

• Thoracic outlet syndrome
• Genes
• Mutations