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Co-occurrence of sickle cell disease and oculocutaneous albinism in a Congolese patient: a case report
BACKGROUND: Sickle cell disease and oculocutaneous albinism are rare autosomal recessive disorders both related to mutations on chromosome 11. The diagnosis of patients suffering from both pathologies is necessary to enable dedicated monitoring of any complications at the ophthalmic and skin level....
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686233/ https://www.ncbi.nlm.nih.gov/pubmed/34924007 http://dx.doi.org/10.1186/s13256-021-03214-5 |