Results 41 to 50 of about 1,222,414 (189)

Kartagener's syndrome

open access: yesThe Lancet, 2009
By means of in-vitro fertilisation and embryo transfer an epileptic married Qatari female with Kartagener's syndrome bore two sons, both of whom were haemophiliac. The nature of Kartagener's syndrome audits implications are explained and discussed.
Vinay, Kapur   +3 more
openaire   +3 more sources

Right Bochdalek Hernia Associated with Kartagener Syndrome: Developmental and Clinical Observations

open access: yesEuropean Journal of Pediatric Surgery Reports, 2013
We present a novel case of the association of right-sided Bochdalek hernia, a diaphragmatic life-threatening malformation, and Kartagener syndrome, which is characterized by congenital bronchiectasis, chronic sinusitis, and situs inversus.
Carmelo Romeo   +4 more
doaj   +1 more source

Kartagener syndrome with renal amyloidosis: a case report [PDF]

open access: yes, 2023
Kartagener syndrome is a rare disorder caused by defective ciliary function. It is described as a triad of cystic bronchiectasis, chronic sinusitis, and situs invertus. Renal involvement, although uncommon, is reported.
Naredi, Mohit   +3 more
core   +1 more source

International Collaboration in Primary Ciliary Dyskinesia

open access: yesPediatric Pulmonology, Volume 61, Issue 11, November 2026.
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

PIH1D2 Loss‐of‐Function Directs Ciliary and Cell Cycle Defects Resulting in Left Isomerism With or Without Biliary Atresia

open access: yesLiver International, Volume 46, Issue 11, November 2026.
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

Open Cholecystectomy in a Patient With Situs Inversus Totalis and Symptomatic Cholelithiasis: A Case Report

open access: yesClinical 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

KARTAGENER SYNDROME [PDF]

open access: yes, 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  

Living Donor Liver Transplantation in Pediatric Situs Inversus: A Case Series and Systematic Review

open access: yesPediatric 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

Laparoscopic Cholecystectomy in Kartagener Syndrome

open access: yes, 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

Nasal obstruction and productive cough in a 12 years old girl in Basrah, Iraq; the diagnosis of Kartagener syndrome is established. [PDF]

open access: yes, 2022
Kartagener syndrome (KS) is an autosomal recessive genetic disorder characterized by ciliary dyskinesia that causes defects in the action of ciliary movement affecting the nose, paranasal sinuses, lung and others.
Haider Kadhem Saeed   +1 more
core   +1 more source

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