DSpace@İnönü

Renal failure in a patient with autosomal dominant polycystic kidney

Basit öğe kaydını göster

dc.contributor.author Bahceci, F
dc.contributor.author Sari, R
dc.contributor.author Sarikaya, M
dc.contributor.author Atik, E
dc.contributor.author Karincaoglu, Y
dc.contributor.author Sevinc, A
dc.date.accessioned 2022-03-14T07:38:28Z
dc.date.available 2022-03-14T07:38:28Z
dc.date.issued 2004
dc.identifier.uri http://hdl.handle.net/11616/55192
dc.description.abstract Autosomal dominant polycystic kidney disease is a multisystem disorder characterized by multiple, bilateral renal cysts and is also associated with cysts in other organs, such as the liver, pancreas, and arachnoid membranes. Dermatomyosiltis is a disease which mainly involves the skin and muscles, although occasionally other organs are affected. In this report, a 56-year-old male patient with a four-year history of autosomal dominant polycystic kidney disease was presented. Renal failure was exacerbated by a coexisting dermato-polymyositis. Prednisone treatment with hemodialysis improved the situation. This is the first report renal failure in a patient with autosomal dominant polycystic kidney disease and dermato-polymyositis.
dc.source JOURNAL OF THE NATIONAL MEDICAL ASSOCIATION
dc.title Renal failure in a patient with autosomal dominant polycystic kidney
dc.title disease and coexisting dermato-polymyositis: First report in the
dc.title literature


Bu öğenin dosyaları:

Dosyalar Boyut Biçim Göster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster