[HTML][HTML] Polycystic kidney disease, autosomal dominant

PC Harris, VE Torres - 2018 - europepmc.org
Autosomal dominant polycystic kidney disease (ADPKD) is generally a late-onset
multisystem disorder characterized by bilateral kidney cysts, liver cysts, and an increased …

Implementation of rapid genome sequencing for critically ill infants with complex congenital heart disease

T Hays, R Hernan, M Disco, EL Griffin… - Circulation: Genomic …, 2023 - Am Heart Assoc
BACKGROUND: Rapid genome sequencing (rGS) has been shown to improve care of
critically ill infants. Congenital heart disease (CHD) is a leading cause of infant mortality and …

Management of Hypertension and Associated Cardiovascular Disease in Autosomal Dominant Polycystic Kidney Disease

FF Rahbari-Oskoui - Advances in Kidney Disease and Health, 2023 - Elsevier
Autosomal dominant polycystic kidney disease is the most commonly inherited disease of
the kidneys affecting an estimated 12,000,000 people in the world. Autosomal dominant …

Renal denervation helps preserve the ejection fraction by preserving endocardial-endothelial function during heart failure

S Pushpakumar, M Singh, Y Zheng… - International Journal of …, 2023 - mdpi.com
Renal denervation (RDN) protects against hypertension, hypertrophy, and heart failure (HF);
however, it is not clear whether RDN preserves ejection fraction (EF) during heart failure …

Case report: A novel occurrence of persistent left cranial vena cava coexisting with polycystic kidney disease in a cat

YE Cha, WB Ro, SJ Song, MK Lee, MH Kang… - Frontiers in Veterinary …, 2023 - frontiersin.org
A 7-year-old castrated male Munchkin cat was presented with anorexia. This cat had been
diagnosed with chronic kidney disease due to polycystic kidney disease. Tachycardia with a …

Monoallelic loss-of-function IFT140 pathogenic variants cause autosomal dominant polycystic kidney disease: a confirmatory study with suspicion of an additional …

S Salhi, A Doreille, MS Dancer, A Boueilh… - American Journal of …, 2024 - Elsevier
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited
kidney disease. While biallelic variants affecting IFT140 are responsible for Mainzer-Saldino …

Overview of clinical status, treatment, and long-term outcomes of pediatric autosomal-dominant polycystic kidney disease: a nationwide survey in Taiwan

CY Chin, WT Huang, JH Wang, JW Liou, HJ Hsu… - Scientific Reports, 2024 - nature.com
This retrospective study investigated the incidence, medication use, and outcomes in
pediatric autosomal-dominant polycystic kidney disease (ADPKD) using Taiwan's National …

Isolated double orifice mitral valve in a patient with autosomal dominant polycystic kidney disease

K Digrande, J Xu, EH Dineen, AY Lee - CASE, 2023 - cvcasejournal.com
Isolated Double Orifice Mitral Valve in a Patient With Autosomal Dominant Polycystic Kidney
Disease - CASE Skip to Main Content Skip to Main Menu Advertisement CASE Log in ASE …

Extrarenal clinical features are reported for most genes implicated in genetic kidney disease

B Serrano, J Savige - 2024 - researchsquare.com
Background: Genetic kidney disease is typically suspected where there is a positive family
history or extrarenal features. This study examined how often these criteria might be …

Autosomal dominant polycystic kidney disease (ADPKD): Extrarenal manifestations

WM Bennett, VE Torres - uptodate.com
INTRODUCTION—Autosomal dominant polycystic kidney disease (ADPKD) is characterized
by cysts in the kidneys and, in many cases, is associated with cysts in the liver and pancreas …