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

RATIONALE: 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,...

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Detalles Bibliográficos
Autores principales: Zhang, Qi-Jie, Xu, Liu-Qing, Wang, Chong, Hu, Wei, Wang, Ning, Chen, Wan-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265983/
https://www.ncbi.nlm.nih.gov/pubmed/27930511
http://dx.doi.org/10.1097/MD.0000000000005331

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265983/
https://www.ncbi.nlm.nih.gov/pubmed/27930511
http://dx.doi.org/10.1097/MD.0000000000005331

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