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Wilson disease

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Hypercalciuria

Total: 1

(per page)

PMID (PMCID)
2744017	MALE	Child
	Hypercalciuria and nephrolithiasis as a presenting sign in Wilson disease.
	Azizi E, Eshel G, Aladjem M. Eur J Pediatr. 1989;148(6):548-9.
	Hypercalciuria and nephrolithiasis as a presenting sign in Wilson disease.