Wilson’s Disease and Nevus of Ota in a Child: A Case Report.

<bold><italic>Introduction:</italic></bold> 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 of Ota, is a painless condition characterized by hyperpigmentation in and around the eye. In this case report, we describe the unique occurrence of both conditions in this pediatric patient. <bold><italic>Case Presentation:</italic></bold> A 10-year-old girl exhibited classic ocular signs associated with Wilson’s disease, including Kayser-Fleischer rings and sunflower-type cataracts. Additionally, she displayed unilateral confluent gray-blue hyperpigmentation consistent with a nevus of Ota. As of now, the patient remains asymptomatic, with preserved visual acuity. <bold><italic>Conclusions:</italic></bold> To the best of our knowledge, this case represents the first report of nevus of Ota in a child diagnosed with Wilson’s disease. [ABSTRACT FROM AUTHOR]