Unusual presentation of Wilson's disease in children: recurrent gross hematuria

Authors

  • R Ben Rabeh (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • A Ben Ismail (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • O Bouyahia (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • N Missaoui (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • S Atitallah (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • S Yahyaoui (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • S Mazigh (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author
  • S Boukthir (1) University Tunis El Manar, Faculty of medicine of Tunis, Tunisia; (2) Pediatric Department C, Bechir Hamza Children's hospital Tunis, Tunisia Author

Keywords:

Wilson's disease, ATP7B gene, gross hematuria, hypercalciuria, kidney stones, Child

Abstract

Wilson's disease is an autosomal recessive inherited disorder of copper metabolism. It has a variety of presentations. We reported a case of 14-year-old boy who presented with a history of recurrent macroscopic hematuria and flank pain. He had signs of chronic liver disease and dysarthria. He had kidney stones and hypercalciuria. The diagnosis of Wilson's disease was confirmed by low serum ceruloplasmin level, high 24 hours urinary copper excretion and genetic testing.

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Published

2022-09-30