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....

Descripción completa

Detalles Bibliográficos
Autores principales: Mbiya Mukinayi, Benoît, Mpoyi Kalenda, John, Kalombo Kalenda, Didier, Disashi Tumba, Ghislain, Gulbis, Béatrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
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

Internet

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

Ejemplares similares