Results 51 to 60 of about 570 (99)

New Treatments Are Urgently Needed for Patients With All Primary Ciliary Dyskinesia Genotypes

open access: yes
Pediatric Pulmonology, Volume 60, Issue 11, November 2025.
Benjamin Gaston   +10 more
wiley   +1 more source

Primary ciliary dyskinesiatwo cases reports

open access: yesJournal of Mazandaran University of Medical Sciences, 2009
(Received 22 December, 2009 ; Accepted 10 March, 2010)AbstractPrimary ciliary dyskinesia and Kartagener's syndrome are rare genetic disorders. There is a ciliary dysfunction in these disorders that cause recurrent infections in respiratory and sinus ...
Mohammad Sadegh Rezaee1   +3 more
doaj  

Unveiling Kartagener’s Syndrome in a Young Male: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Kartagener's Syndrome (KS) is a rare genetic condition that affects the cilia. It is characterised by a situs inversus triad, chronic sinusitis, and bronchiectasis, distinguishing it from other diseases.
Priyanka Kalpesh Negandhi   +4 more
doaj   +1 more source

Bone marrow involvement of a patient with Niemann-Pick disease concomitant with Kartagener’s syndrome: Report of a rare case

open access: yesMediterranean Journal of Hematology and Infectious Diseases, 2014
Niemann-Pick disease is a rare lipid storage disorder with autosomal recessive inheritance, which is characterized by accumulation of sphingomyelin and other sphingolipids in macrophages. In most cases, macrophage lipids show a non-spesific, ?ntense blue
Muzaffer Keklik   +7 more
doaj  

Primary ciliary dyskinesia (Siewert's / Kartagener's Syndrome): Respiratory symptoms and psycho-social impact

open access: yesBMC Pulmonary Medicine, 2003
Background Although the pathophysiological defect in primary ciliary dyskinesia (PCD; Siewert's / Kartagener's syndrome) is now well characterised, there are few studies of the impact of the condition upon health function, particularly in later life ...
Stubbings Georgina F   +4 more
doaj   +1 more source

Anesthetic Management of Dextrocardia with Situs Inversus for Caesarean Section- A Case Report

open access: yesSiriraj Medical Journal, 2016
Dextrocardia is a congenital cardiac malrotation in which the heart is situated on the right side of the body (dextroversion) with the apex pointing to the right. It may be associated with many cardiac and non-cardiac anomalies.
Rakesh Karnawat
doaj   +2 more sources

A Novel Potentially Pathogenic DNAH5 Variant in a Patient with Kartagener’s Syndrome from Ardabil Province: A Case Report [PDF]

open access: yesJournal of Mazandaran University of Medical Sciences
Kartagener's syndrome is a rare autosomal recessive genetic disorder characterized by a clinical triad: chronic sinusitis, bronchiectasis, and situs inversus.
Atabak Sedigh-Namin   +4 more
doaj  

Relationship Between Kartagener’s Syndrome and Internal Diseases: Coincidence or Coexistence

open access: yesJournal of Contemporary Medicine
Kartagener’s syndrome (KS) is included in the group of diseases arising from primary ciliarydyskinesia (PCD) and is characterized by the triad of situs inversus, chronic sinusitis andbronchiectasis.Patients with PCD, including KS, may present with ...
Muhammet Limon, Nurdan Yıldırım
doaj   +1 more source

Siewert-Kartagener's syndrome in a dog. [PDF]

open access: yesJ Vet Sci, 2023
Jung R   +5 more
europepmc   +1 more source

Anaesthetic implications in situs inversus totalis: a case report

open access: yesJournal of the Pakistan Medical Association
Situs inversus totalis (SIT) is a rare congenital condition which is characterised by the reversal of orientation of abdominal and thoracic organs where heart is on the right side of the thoracic cavity and liver on the left side, whereas stomach and ...
Faraz Mansoor   +2 more
doaj   +1 more source

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