遗传性扭转性肌张力障碍所致横纹肌溶解症
Rhabdomyolysis due to hereditary torsion dystonia.
作者信息
Paret G, Tirosh R, Ben-Zeev B, Vardi A, Brandt N, Barzilay Z
机构信息
Pediatric ICU, Chaim Sheba Medical Center, Tel Hashomer, Israel.
出版信息
Pediatr Neurol. 1995 Jul;13(1):83-4. doi: 10.1016/0887-8994(95)00111-r.
PMID:7575858
Abstract
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.
摘要
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。
相似文献
1
Rhabdomyolysis due to hereditary torsion dystonia.遗传性扭转性肌张力障碍所致横纹肌溶解症
Pediatr Neurol. 1995 Jul;13(1):83-4. doi: 10.1016/0887-8994(95)00111-r.
2
Torsion dystonia.扭转性肌张力障碍
Curr Opin Neurol. 1996 Aug;9(4):317-20. doi: 10.1097/00019052-199608000-00014.
3
A familial study in serum dopamine-beta-hydroxylase levels in torsion dystonia.
Neurology. 1974 Jul;24(7):684-7. doi: 10.1212/wnl.24.7.684.
4
The relationship between trauma and idiopathic torsion dystonia.创伤与特发性扭转性肌张力障碍之间的关系。
J Neurol Neurosurg Psychiatry. 1991 Aug;54(8):713-7. doi: 10.1136/jnnp.54.8.713.
5
Dystonia in 61-year-old identical twins: observations over 45 years.61岁同卵双胞胎的肌张力障碍：45年观察记录
Ann Neurol. 1984 Sep;16(3):356-8. doi: 10.1002/ana.410160313.
6
The autosomal dominant dystonias.常染色体显性肌张力障碍
Brain Pathol. 1992 Oct;2(4):297-308. doi: 10.1111/j.1750-3639.1992.tb00707.x.
7
Variable onset of adult inherited focal dystonia: a problem for genetic studies.成人遗传性局灶性肌张力障碍的发病时间多变：对遗传学研究来说是个问题。
Mov Disord. 1994 Jan;9(1):64-8. doi: 10.1002/mds.870090110.
8
Evidence for locus heterogeneity in autosomal dominant torsion dystonia.常染色体显性扭转性肌张力障碍中基因座异质性的证据。
Genomics. 1993 Jan;15(1):9-12. doi: 10.1006/geno.1993.1003.
9
Tiapride as treatment for certain patients with idiopathic torsion dystonia.硫必利作为某些特发性扭转性肌张力障碍患者的治疗方法。
Eur Neurol. 1991;31(6):356-9. doi: 10.1159/000116693.
10
Molecular genetics of an autosomal dominant form of torsion dystonia.常染色体显性扭转肌张力障碍的分子遗传学
Adv Neurol. 1988;50:57-66.
引用本文的文献
1
Movement disorder emergencies.运动障碍急症
J Neurol. 2008 Aug;255 Suppl 4:2-13. doi: 10.1007/s00415-008-4002-9.
2
Movement disorder emergencies.运动障碍急症
Curr Neurol Neurosci Rep. 2005 Jul;5(4):284-93. doi: 10.1007/s11910-005-0073-5.
Zotero 插件