Abstract
Wilson’s disease, an autosomal recessive disorder of copper metabolism, most commonly presents either with hepatic or neurological features. sometimes it may have certain atypical features like cutaneous and renal manifestations which may lead to diagnostic difficulties. we report here a case of Wilson disease who presented as Xerosis and generalised hyperpigmentation of body along with nephrotic range proteinuria. This case report is rare and highlights the fact that early recognition of skin lesions may play a role in diagnosis of Wilson’s disease and specific treatment can prevent further liver injury and neurological complications in most cases.
Keywords: xerosis, hyperpigmentation, Wilson’s disease, proteinuria.
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Corresponding Author
Samar Pratim Nayak
Department of Pediatrics, SVPPGIP, SCB Medical College, Cuttack
DOI: https://dx.doi.org/10.18535/jmscr/v11i6.15
