在一个12岁男孩的急性脑病和耐火性低血清症

Toktam Moosavian1, Zahra Pournasiri2, Shiva Fatollahierad2

  • 1Pediatric Neurology Department, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

PubMed
概括

威尔逊病是一种遗传性铜过载障碍,可以出现神经和脏问题. 即使肝功能正常,通过切鲁洛普拉斯和尿铜测试进行早期诊断至关重要.

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