Results 41 to 50 of about 1,136,166 (186)
The Pan African Medical Journal, 2019 Le syndrome de Kartagener est une entité particulière parmi les dyskinésies ciliaires primitives (DCP) caractérisée par une triade clinique: sinusite, bronchectasie et situs inversus complet ou incomplet. C'est une maladie congénitale rare à transmission
Amadou Doumbia +4 more
doaj +1 more source
Síndrome de Kartagener em um cão (Canis lupus familiaris) da raça Cocker Spaniel Inglês
Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 2011 Kartagener is syndrome is a rare disorder described in dogs determined by the triad situs inversus totalis, chronic sinusitis, and bronchial disease. The clinical signs of chronic respiratory and other less common presentations (such as hydrocephalus and
P. Souza Junior +2 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT Situs inversus totalis (SIT) reverses normal anatomical landmarks used during cholecystectomy, requiring careful preoperative imaging, a mirror‐image surgical strategy, and strict achievement of the critical view of safety before ductal or vascular division.
Syeda Farwa Parihan Gillani +5 more
wiley +1 more source
A woman with recurrent respiratory tract infections
The Pan African Medical Journal, 2020 A 76-year-old Caucasian woman who has been repeatedly hospitalized with recurrent respiratory tract infections, presented to the emergency department with fever and productive cough during the last 24 hours.
Petros Ioannou
doaj +1 more source
Children, 2023 The goal of this manuscript is to present and summarize several rare pediatric syndromes (Zellweger syndrome, Kartagener syndrome, Prader-Willi syndrome, Schinzel-Giedion syndrome, Fanconi anemia, Joubert-Boltshauser syndrome, Poretti-Boltshauser ...
Laura M. Huisman +1 more
doaj +1 more source
Living Donor Liver Transplantation in Pediatric Situs Inversus: A Case Series and Systematic Review
Pediatric Transplantation, Volume 30, Issue 8, August 2026.ABSTRACT Liver transplantation (LT) in patients with situs inversus (S‐I) is rare and technically challenging. The literature on such cases, particularly in pediatric populations, remains limited. Here, we report the surgical considerations and outcomes of two pediatric recipients with situs inversus abdominalis who underwent liver transplantation for ...
Maria F. Fernandez +19 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.We report pseudo‐dominant PCD inheritance in a Chinese family due to novel DNAAF1 mutations. Affected members across two generations showed significant variability in lung disease progression and visceral arrangement. ABSTRACT Background Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder typically inherited in an autosomal ...
Zhuoyao Guo +3 more
wiley +1 more source
, 2010 Kartagener sendromu otozomal resesif geçişli sinüzit, bronşektazi, situs inversus ile karakterize ender görülen bir hastalıktır. Bu makalede, kliniğimizde Kartagener sendromu tanısı ile izlediğimiz iki olgunun klinik ve radyolojik bulguları verilmiştir ...
KARAMAN, ÖZKAN +5 more
core
Laparoscopic Cholecystectomy in Kartagener Syndrome
, 2017 Kartagener syndrome is a rare autosomal recessive disorder in which there is situs inversus involving abdominal or thoracic viscera or both. Anatomy of the abdominal organs in such a patient is distorted making laparoscopic surgery very difficult.
Ganga R Verma +2 more
core +1 more source
Frontiers in Genetics, 2020 Introduction: Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease characterized by structural or functional motile cilia abnormalities. Up to 40 different genes seem, at the moment, to be involved in the pathogenesis of PCD.
Rossella Cannarella +7 more
doaj +1 more source