Co-occurrence of sickle cell disease and oculocutaneous albinism in a Congolese patient: a case report

Journal of Medical Case Reports

Béatrice Gulbis¹  Ghislain Disashi Tumba²  Benoît Mbiya Mukinayi³  Didier Kalombo Kalenda³  John Mpoyi Kalenda⁴ 

[1]Clinical Chemistry Department, Hereditary Red Blood Cell Disorders, LHUB-ULB, Université Libre de Bruxelles, 1070, Brussels, Belgium

[2]Internal Medicine Department, Faculty of Medicine, University of Mbujimayi, 06201, Mbuji-Mayi, Democratic Republic of Congo

[3]Pediatrics Department, Faculty of Medicine, University of Mbujimayi, 06201, Mbuji-Mayi, Democratic Republic of Congo

[4]Sickle Cell Reference Center, Clinique Pédiatrique de Mbujimayi, Pediatrics Clinic of Mbujimayi, 06201, Mbuji-Mayi, Democratic Republic of Congo

[5]Sickle Cell Reference Center, Clinique Pédiatrique de Mbujimayi, Pediatrics Clinic of Mbujimayi, 06201, Mbuji-Mayi, Democratic Republic of Congo

关键词: Sickle cell disease;    Oculocutaneous albinism;    Mbujimayi;    Democratic Republic of the Congo;   

DOI  :  10.1186/s13256-021-03214-5

来源: Springer

【 授权许可】

CC BY