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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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| Pubblicato in: | Medicine (Baltimore) |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wolters Kluwer Health
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6320091/ https://ncbi.nlm.nih.gov/pubmed/30558096 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000013744 |
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