Wilson disease patient with rare heterozygous mutations in ATP7B accompanied by distinctive nocturnal enuresis: A case report

INTRODUCTION: Wilson disease (WD) is an autosomal-recessive disorder of copper metabolism, which exhibits various symptoms due to the combination of environmental and genetic factors. Here, we report a WD patient who displayed distinctive symptom of nocturnal enuresis. PATIENT CONCERNS: The patient...

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Detalles Bibliográficos
Autores principales: Zhang, Shijie, Li, Liangyong, Wang, Jiuxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360279/
https://www.ncbi.nlm.nih.gov/pubmed/32664103
http://dx.doi.org/10.1097/MD.0000000000020997

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360279/
https://www.ncbi.nlm.nih.gov/pubmed/32664103
http://dx.doi.org/10.1097/MD.0000000000020997

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