Ontology highlight
ABSTRACT:
SUBMITTER: Massella L
PROVIDER: S-EPMC5989684 | biostudies-literature | 2018 Jun
REPOSITORIES: biostudies-literature
Massella Laura L Mekahli Djalila D Paripović Dušan D Prikhodina Larisa L Godefroid Nathalie N Niemirska Anna A Ağbaş Ayşe A Kalicka Karolina K Jankauskiene Augustina A Mizerska-Wasiak Malgorzata M Afonso Alberto Caldas AC Salomon Rémi R Deschênes Georges G Ariceta Gema G Özçakar Z Birsin ZB Teixeira Ana A Duzova Ali A Harambat Jérôme J Seeman Tomáš T Hrčková Gabriela G Lungu Adrian Catalin AC Papizh Svetlana S Peco-Antic Amira A De Rechter Stéphanie S Giordano Ugo U Kirchner Marietta M Lutz Teresa T Schaefer Franz F Devuyst Olivier O Wühl Elke E Emma Francesco F
Clinical journal of the American Society of Nephrology : CJASN 20180419 6
<h4>Background and objectives</h4>Autosomal dominant polycystic kidney disease is the most common inheritable kidney disease, frequently thought to become symptomatic in adulthood. However, patients with autosomal dominant polycystic kidney disease may develop signs or symptoms during childhood, in particular hypertension. Although ambulatory BP monitoring is the preferred method to diagnose hypertension in pediatrics, data in children with autosomal dominant polycystic kidney disease are limite ...[more]