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Kartagener's syndrome is a subdivision of primary ciliary dyskinesia (PCD)/immotile-cilia syndrome that includes situs inversus, bronchiectasis, sinusitis, and infertility. Although the symptoms appear early, it remains undiagnosed for years.
Vasavi Sri Dattasena Rudraraju +3 more
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Kartagener’s Syndrome Presenting As Bilateral Recurrent Nasal Polyposis In A Young Boy
Kartagener's syndrome is a very rare congenital disease consists of a classic triad, sinusitis, situs inversus and bronchiectasis. Approximately one half of patients with primary ciliary dyskinesia have situs inversus and Kartagener syndrome.
Zeba Ahmed, Warda Waseem, Uroosa Saman
doaj +1 more source
Kartagener syndrome with pectus excavatum and upper lobar bronchiectasis
Primary Ciliary Dyskinesia (PCD) is a rare autosomal recessive disorder caused by impaired ciliary function. The incidence of PCD is 1 in 20,000 births. Kartagener's syndrome (KS), a subtype of PCD, is distinguished by the presence of situs inversus.
Zain Saleem Khan, MD +4 more
doaj +1 more source
Kartagener’s Syndrome and Psychotic Disorder: A Case Presentation [PDF]
Kartagener’s syndrome is a rare congenital malformation and characterized by the triad of bronchiectasis, sinusitis, and situs inversus. We presented a case diagnosed as Kartagener’s syndrome and psychotic disorder.
Ayşegül Ermiş +3 more
doaj
Renal Carcinoma and Kartagener Syndrome: An Unusual Association
Background. The association of renal cell carcinoma and Kartagener’s syndrome is unusual, and only eleven cases have been reported in the literature. The purpose of this work is to analyze this unusual association of Kartagener’s syndrome and renal cell ...
Hamza Dergamoun +5 more
doaj +1 more source
International Collaboration in Primary Ciliary Dyskinesia
ABSTRACT Primary Ciliary Dyskinesia (PCD) exemplifies how international collaboration can transform the study of a rare disease. Since the identification of the first PCD‐associated genes in 1999–2002, parallel developments in Europe and North America, driven by patient organizations, academic investigators, and coordinated funding initiatives, have ...
Petra Pennekamp +2 more
wiley +1 more source
ABSTRACT Background & Aims Laterality disorders are rare congenital conditions caused by disruption of left–right embryonic patterning, often associated with ciliary dysfunction. Despite the identification of numerous causative genes, the molecular basis remains unresolved in many patients.
Alina Kurolap +19 more
wiley +1 more source
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
Living Donor Liver Transplantation in Pediatric Situs Inversus: A Case Series and Systematic Review
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
Kartagener's syndrome presenting with secondary spontaneous pneumothorax: A rare case report
Kartagener's syndrome (KS) is a part of a larger family of diseases classified as primary ciliary dyskinesia (PCD). The triad of KS consists of bronchiectasis, chronic sinusitis, and situs inversus, which is likely underdiagnosed, as a limited amount of ...
Niranjan Prabhakar +2 more
doaj +1 more source

