A case report: Co-occurrence of Wilson disease and oculocutaneous albinism in a Chinese patient

RATIONALE: Both Wilson disease (WD) and Oculocutaneous Albinism (OCA) are rare autosomal recessive disorders that are caused by mutations on chromosome 13 and chromosome 11, respectively. Here, we report on a patient with coexisting WD and OCA, initially presenting episodes of tremors. PATIENT CONCE...

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Detalles Bibliográficos
Autores principales: Rao, Rao, Shu, Shan, Han, Yong Zhu, Chiu, Yu-Jen, Han, Yong Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320091/
https://www.ncbi.nlm.nih.gov/pubmed/30558096
http://dx.doi.org/10.1097/MD.0000000000013744

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320091/
https://www.ncbi.nlm.nih.gov/pubmed/30558096
http://dx.doi.org/10.1097/MD.0000000000013744

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