[Autosomal dominant polycystic kidney disease]

التفاصيل البيبلوغرافية
العنوان: [Autosomal dominant polycystic kidney disease]
المؤلفون: Signe Vinsand, Naver, Bjarne, Ørskov, Anja Møller, Jensen, Martin, Egfjord
المصدر: Ugeskrift for laeger. 179(24)
سنة النشر: 2017
مصطلحات موضوعية: Adult, Diagnosis, Differential, Male, Young Adult, TRPP Cation Channels, Adolescent, Humans, Female, Middle Aged, Polycystic Kidney, Autosomal Dominant, Magnetic Resonance Imaging, Aged
الوصف: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disorder which causes end stage renal disease. In Denmark, estimated 5,000 patients are living with the disease. Most of the patients are in regular contact with physicians due to the progression of kidney failure causing hypertension as well as cyst infections, back pain, abdominal distension and other symptoms caused by the enlarged kidneys. In this article we describe the clinical presentation, the genetics, the pathophysiology and the current and future treatment modalities of the disease.
تدمد: 1603-6824
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::ed197ee45311ce3789373f86f46d9b36Test
https://pubmed.ncbi.nlm.nih.gov/28606296Test
رقم الانضمام: edsair.pmid..........ed197ee45311ce3789373f86f46d9b36
قاعدة البيانات: OpenAIRE