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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.

Metabolic acidosis

Acid accumulation or depletion of base in the body due to buildup of metabolic acids.

Total: 1

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PMID (PMCID)
19246413	MALE
	Recurrent limb weakness in a 17-year-old boy.
	Thapa R, Biswas B, Mallick D. Clin Pediatr (Phila). 2009;48(5):555-7.
	Careful search of an underlying etiology in children presenting with hypokalemic weakness of the limbs in the face of metabolic acidosis and unexplained hepatitis may reveal Wilson disease.