Surgical resection of multiple angiomatous lesions of the limbs in an 11-year-old girl with beals syndrome: a case report
Background: Beals syndrome, or congenital contractural arachnodactyly (CCA), is a rare autosomal dominant connective tissue disorder caused by pathogenic variants of FBN2. The association with diffuse vascular malformations is exceptional. Airway management during anesthesia is challenging due to joint contractures and restricted cervical mobility. Case presentation: We report the case of an 11-year-old girl with genetically confirmed Beals syndrome who underwent resection of multiple angiomatous lesions of the limbs.