Alport syndrome is a genetic disorder primarily affecting the kidneys, eyes, and ears, characterised by a classical triad of haematuria, anterior lenticonus, and sensorineural deafness. This case series examines the ocular manifestations, particularly posterior lenticonus, in three patients with Alport syndrome evaluated at a tertiary care centre. By integrating current findings from recent studies, this series highlights the significance of ophthalmic assessment in diagnosing and managing Alport syndrome.
Toshniwal et al. (Sat,) studied this question.