Morbo di Wilson: certezze e ancora tanti dubbi!

Wilson’s disease: certainties and still doubts

Fabiola Di Dato, Raffaele Iorio

Dipartimento di Scienze Mediche Traslazionali, Sezione di Pediatria, Università degli Studi di Napoli Federico II

Wilson’s Disease (WD) is a rare genetic disorder of copper metabolism. Although WD has been known for more than 100 years, due to its rarity, it still has many controversial points from a diagnostic and therapeutic point of view, even more in children than in adults. Here, through a systematic review, we try to answer the main critical issues.

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