Four-year follow-up of a Wilson disease pedigree complicated with epilepsy and hypopituitarism: Case report with a literature review

Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism with excellent prognosis if treated timely. However, WD is usually prone to neglect and misdiagnosis at an early stage. We reported a rare WD pedigree, and the clinical features, laboratory tests, and gene m...

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Veröffentlicht in:Medicine (Baltimore) 2016-12, Vol.95 (49), p.e5331-e5331
Hauptverfasser: Zhang, Qi-Jie, Xu, Liu-Qing, Wang, Chong, Hu, Wei, Wang, Ning, Chen, Wan-Jin
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Sprache:eng
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