Background: Loeys-Dietz syndrome (LDS), an autosomal-dominant connective tissue disorder, is characterised by systemic manifestations including arterial aneurysm and craniofacial dysmorphologies. Although ocular involvement in LDS has been reported, detailed information on those manifestations is lacking.
Methods: Retrospective chart review of patients with diagnosed LDS and comparison with age-matched control patients.
Background: To study biometric and structural ocular manifestations of Marfan syndrome (MFS).
Methods: Observational, retrospective, comparative cohort study in a tertiary referral center on 285 MFS patients and 267 controls. Structural and biometric ocular characteristic were compared.