Paret G, Tirosh R, Ben-Zeev B, Vardi A, Brandt N, Barzilay Z
Pediatric ICU, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Pediatr Neurol. 1995 Jul;13(1):83-4. doi: 10.1016/0887-8994(95)00111-r.
Following an acute dystonic crisis, a 6-year-old boy with hereditary torsion dystonia developed rhabdomyolysis. To our knowledge, hereditary torsion dystonia has never been reported as a cause of rhabdomyolysis. Early diagnosis and treatment of rhabdomyolysis should be considered in children with severe dystonia in order to prevent renal failure.
在一次急性肌张力障碍危象后，一名患有遗传性扭转性肌张力障碍的6岁男孩发生了横纹肌溶解症。据我们所知，遗传性扭转性肌张力障碍从未被报道为横纹肌溶解症的病因。对于患有严重肌张力障碍的儿童，应考虑早期诊断和治疗横纹肌溶解症，以预防肾衰竭。
