Results 71 to 80 of about 7,592 (174)
British Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 3037-3048, September 2026.Abstract Aim Besides registries, healthcare databases can provide useful information for assessing the frequency of major congenital malformations (MCMs) and investigating their risk factors, particularly medication exposures. This study aimed to assess the validity of MCMs identification based on French national, comprehensive healthcare databases ...
Tom Duchemin +7 more
wiley +1 more source
Horseshoe kidney transplantation
Interventional Medicine and Applied Science, 2015 Horseshoe kidney is a fusion anomaly found in approximately one in 400–600 people. Due to vascular and ureteral variations, transplantation with a horseshoe kidney presents a technical challenge. In our case, the isthmus connected the upper poles and contained parenchyma.
Nemes, BalĂĄzs +7 more
openaire +3 more sources
Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies
Journal of Cell Communication and Signaling, Volume 20, Issue 3, September 2026.This review elucidates the molecular mechanisms and aberrant signaling pathways in renal ciliopathies, links genetic heterogeneity to clinical phenotypes, and lays a theoretical basis for prenatal diagnosis and novel therapies. Abstract Renal ciliopathies encompass a spectrum of genetic disorders arising from structural or functional impairments of ...
Qiaowei Zhang +7 more
wiley +1 more source
A Hypertensive Patient With Polycystic Horseshoe Kidney
Turkish Journal of Nephrology, 2019 Adult polycystic kidney disease is transmitted in autosomal dominant pattern with a reported incidence of 1 in 1000 to 1 in 5000 cases. Horseshoe kidney is a renal fusion anomaly with an incidence of 1 in 400 to 1 in 1800 live births.
Alper KIRKPANTUR +3 more
doaj
Journal of Medical Case ReportsBackground Horseshoe kidney is the most common renal fusion anomaly, occurring in approximately 1 in 500 individuals worldwide. It is characterized by abnormalities in kidney position, rotation, and vascular supply.
Philipo Felix Mwita +7 more
doaj +1 more source
Muscle &Nerve, Volume 74, Issue S1, Page S31-S40, September 2026.ABSTRACT Congenital myasthenic syndromes (CMS) are inherited disorders caused by mutations in genes encoding proteins essential for neuromuscular junction (NMJ) function. Pathogenic variants have been identified in more than 35 genes, underscoring the complexity of synaptic biology and the wide range of mechanisms that can compromise neuromuscular ...
Rocio‐Nur Villar‐Quiles +5 more
wiley +1 more source
Wildlife Biology, Volume 2026, Issue 5, September 2026.Taxonomic work, conservation practice, and Red List assessments from the International Union for Conservation of Nature (IUCN) are intricately linked. The primary conservation goal for biodiversity is to halt the factors driving local extinctions of species.
Methode Majyambere +4 more
wiley +1 more source
Our Experience in Renal Transplantation from Horseshoe Kidney To Two Recipients: Case Report
Turkish Journal of Nephrology, 2019 Horseshoe kidney is one of the most common congenital fusion anomalies and may be an important option due to the limited donor pool for kidney transplantation.
Oğuz Uğur AYDIN +4 more
doaj
Radiology Case ReportsThe occurrence of triple kidneys, involving a normal kidney and a malrotation horseshoe kidney, is an extremely infrequent condition. This case report demonstrates a triple, mal-rotated horseshoe kidneys coexist with an upper junction stone, alongside a ...
Abdulaziz Hussein, MSc +6 more
doaj +1 more source