...Achia Nemet; Itai Hacker; Chani Topf-Olivestone; Ran Svirsky; Joseph Pikkel; Michael Kinori Introduction: Wilson’s disease is a rare autosomal recessive disorder that disrupts copper metabolism. It presents with distinctive ocular manifestations. Oculodermal melanosis, commonly referred to as nevus...

...Liyung Tiffany Chou; Derek Horkey; Mark Slabaugh Wilson’s disease (WD), also known as hepatolenticular degeneration, is a rare autosomal recessive condition of excess copper accumulation that is most commonly associated with hepatic, neurologic, psychiatric, and ocular manifestations. While Kayser...