Autosomal Recessive Polycystic Kidney Disease in a Child Complicated by Autoimmune Hemolytic Anemia: A Case Report

Autosomal recessive polycystic kidney disease (ARPKD) is a rare genetic disorder that presents as an isolated polycystic renal disease in childhood, or associated with congenital hepatic fibrosis and/or Caroli disease. The spectrum of complications of ARPKD include end stage kidney disease, systemic...

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Autors principals:	Magd A. Kotb, Hend Abd El Baky, Shaimaa Sayed, Mohammed Al Komy, Marwa Onsy, Aya Aly, Andrew Tamer, Esraa Mohamed
Format:	Artigo
Idioma:	Inglês
Publicat:	Cairo University, Faculty of Medicine, Department of Pediatrics 2023-01-01
Col·lecció:	Pediatric Sciences Journal (Egypt)
Matèries:	autosomal recessive polycystic kidney disease autoimmune hemolytic anemia congenital hepatic fibrosis hepatosplenomegaly
Accés en línia:	https://cupsj.journals.ekb.eg/article_252646_e1eb4e8a1e2ab6cc7f8089d1f7a89666.pdf
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