Abstract
An 8-year-old boy with an hepatic form of Wilson disease was treated with oral zinc sulphate as the primary and sole therapy. After 4 months, liver function had dramatically improved, and the parameters characterizing copper metabolism had also normalized.
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Abbreviations
- d-pen:
-
d-penicillamine
- IU:
-
international units
- SCp:
-
serum ceruloplasmin
- SD:
-
standard deviation
- SGGT:
-
serum gamma-glutamyltransferase
- SGOT:
-
serum glutamic-oxalic transaminase
- SGPT:
-
serum glutamic-pyruvic transaminase
References
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Milanino, R., Marrella, M., Moretti, U. et al. Oral zinc sulphate as primary therapeutic intervention in a child with Wilson disease. Eur J Pediatr 148, 654–655 (1989). https://doi.org/10.1007/BF00441526
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DOI: https://doi.org/10.1007/BF00441526