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Early Predictors of Renal Dysfunction in Pediatric Patients with Sickle Cell Disease

Sickle cell disease (SCD) is a hereditary hemoglobinopathy characterized by abnormal hemoglobin production which leads to hemolytic anemia and intermittent occlusion of small blood vessels, which further leads to tissue ischemia, chronic organ damage, and organ dysfunction including urinary system....

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Detalles Bibliográficos
Autores principales: El-Gamasy, Mohamed Abdelaziz, El-Naghy, Wageh S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375016/
https://www.ncbi.nlm.nih.gov/pubmed/30814790
http://dx.doi.org/10.4103/ijn.IJN_40_18