Results 71 to 80 of about 16,967 (166)

Catheter‐Associated Urinary Tract Infections in Children: An Evidence‐Informed Narrative Review of Diagnosis, Management and Prevention

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Catheter‐associated urinary tract infections (CAUTI) are a common healthcare‐associated infection in children and a major contributor to increased morbidity, prolonged hospital stays and higher healthcare costs. This narrative review uses an evidence‐informed approach highlighting recent paediatric literature (2000–2025) to provide an overview
Simon P. Paget, Robert McCusker, Suzanne Simpson, Melissa Short, Angela Berkhout   +4 more
wiley   +1 more source

Periodontal Medicine Rewired: Mechanisms Linking Periodontitis to Systemic Diseases

Journal of Periodontal Research, EarlyView.
This review reorganizes decades of research in periodontal medicine into a multi‐dimensional framework, illustrating how periodontitis influences systemic health through at least seven interconnected mechanisms. ABSTRACT Periodontitis is now recognized not merely as a localized oral condition but as a systemic disease linked to over 70 communicable and
Mario Romandini, George Hajishengallis, Mike Curtis, Giacomo Baima   +3 more
wiley   +1 more source

Repeated versus single praziquantel dosing regimen in treatment of female genital schistosomiasis: a phase 2 randomised controlled trial showing no difference in efficacy

Frontiers in Tropical Diseases
BackgroundSingle-dose praziquantel (PZQ) for treating urogenital schistosomiasis has been reported as inadequate for achieving significant resolution of female genital schistosomiasis (FGS)-associated cervicovaginal lesions.
Louise Thomsen Schmidt Arenholt, Louise Thomsen Schmidt Arenholt, Louise Thomsen Schmidt Arenholt, Bodo Sahondra Randrianasolo, Tiana Onintsoa Oliva Rabozakandraina, Charles Emile Ramarokoto, Karoline Jøker, Katrina Kæstel Aarøe, Dorthe Brønnum, Caspar Bundgaard Nielsen, Suzette Sørensen, Suzette Sørensen, Suzette Sørensen, Mads Lumholdt, Martin Jensen, Søren Lundbye-Christensen, Jørgen Skov Jensen, Paul Corstjens, Pytsje Hoekstra, Govert J van Dam, Noriko Kobayashi, Noriko Kobayashi, Shinjiro Hamano, Shinjiro Hamano, Peter Derek Christian Leutscher, Peter Derek Christian Leutscher   +25 more
doaj   +1 more source

A Case of Persistent Urogenital Sinus: Pitfalls and challenges in diagnosis

Sultan Qaboos University Medical Journal, 2018
Persistent urogenital sinus (PUGS) is a rare anomaly whereby the urinary and genital tracts fail to separate during embryonic development. We report a three-year-old female child who was referred to the Sabah Women & Children Hospital, Sabah, Malaysia ...
Hooi H. Tan, Shung K. Tan, Rajah Shunmugan, Rozman Zakaria, Zakaria Zahari   +4 more
doaj   +1 more source

Urological management in a pediatric patient with mixed gonadal dysgenesis

Urology Case Reports
Disorders of sex development are conditions characterized by alterations in gonadal development that lead to discordance between chromosomal sex, gonadal sex, and phenotypic sex. We report the case of a 4 years old patient with ambiguous genitalia and 45,
Wendy Matilde Chipa Beizaga, Luis José Orbegoso Celis, Brandom Juced Torres Marigorda, Miguel Martín Aguilar Ulloque, Kilder Nicolay García Murga, Valeria Linares Vega, Fernando Jeancarlos Imán Izquierdo, Ronald Aquino-Ortega, Juana del Valle-Mendoza, Wilmer Gianfranco Silva-Caso   +9 more
doaj   +1 more source

Unilateral ductus deferens aplasia with terminal cystic dilation in a Bernese mountain dog

Veterinary Record Case Reports, Volume 14, Issue 3, August 2026.
Abstract An incidental caudal abdominal mass was discovered in a 5‐year‐old, male, entire Bernese mountain dog. Investigations showed a terminal cystic dilation of the left ductus deferens. Castration, along with surgical resection of the mass, was performed, and histopathology of the mass and ductus deferens was consistent with segmental aplasia of ...
Daisy Johnson, Louisa Price, Marie Beales, Joanna Stephenson   +3 more
wiley   +1 more source

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

Testículos supernumerarios: anomalía infrecuente del sistema genital. Reporte de caso

Revista Médica Electrónica
Introducción: El testículo supernumerario es una anomalía congénita urológica poco frecuente, que es definido como la presencia de más de dos testículos, ya sea de localización intra o extraescrotal. Los testículos supernumerarios son una rara anomalía a
Niurka García Sosa, Francisco J Fong Aldama, Rodolfo Santana Valera, Ernesto Toledo Martínez   +3 more
doaj  

An assessment of gynecological manifestations in women with female genital schistosomiasis with reference to Schistosoma biomarkers, sexually transmitted infections and bacterial vaginosis

Frontiers in Tropical Diseases
BackgroundAlthough a variety of different gynecological manifestations have been reported in women with female genital schistosomiasis (FGS), causality remains to be established. This study aimed to evaluate the gynecological manifestations in women with
Bodo Sahondra Randrianasolo, Karoline Jøker, Louise Thomsen Schmidt Arenholt, Louise Thomsen Schmidt Arenholt, Louise Thomsen Schmidt Arenholt, Tiana Onintsoa Oliva Rabozakandraina, Charles Emile Ramarokoto, Dorthe Brønnum, Martin Jensen, Søren Lundbye Christensen, Jørgen Skov Jensen, Paul Corstjens, Govert J. van Dam, Noriko Kobayashi, Noriko Kobayashi, Shinjiro Hamano, Shinjiro Hamano, Peter Derek Christian Leutscher, Peter Derek Christian Leutscher   +18 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source