Journal of Pediatric Neurology 2004; 02(04): 231-233
DOI: 10.1055/s-0035-1557225
Case Report
Georg Thieme Verlag KG Stuttgart – New York

Hyponatremia as a cause of prolonged seizures in a child with sickle cell anemia

Tanıl Kendirli
1   Departments of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey
,
Özlem Ünal
2   Departments of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey
,
Talia İleri
3   Departments of Pediatric Hematology, Ankara University Faculty of Medicine, Ankara, Turkey
,
Mehmet Ertem
3   Departments of Pediatric Hematology, Ankara University Faculty of Medicine, Ankara, Turkey
,
Natalia Sphakova
1   Departments of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey
,
Gülhis Deda
2   Departments of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey
,
Mesiha Ekim
4   Departments of Pediatric Nephrology, Ankara University Faculty of Medicine, Ankara, Turkey
› Author Affiliations

Subject Editor:
Further Information

Publication History

05 February 2004

07 May 2004

Publication Date:
29 July 2015 (online)

Abstract

We report a successful outcome on recurrent hyponatremic seizures, treated with agressive sodium replacement therapy in a 12-year-old girl with sickle cell anemia. The cause of her hyponatremia was probably tubular damage due to vaso-occlusive crisis. We achieved rapid correction in neurologic findings, serum sodium level and urinalysis with sodium replacement and fluid therapy in this patient. We excluded stroke based on the findings in cranial magnetic resonance imaging. We conclude that severe seizures found in sickle cell anemia may result from hyponatremia that can be treated by sodium replacement therapy. (J Pediatr Neurol 2004; 2(4): 231–233).