Kartagener's Syndrome With Complications: Diagnostic Challenges in a Resource‐Limited Setting
Clinical Case ReportsKartagener's Syndrome (KS) is a rare genetic disorder characterized by bronchiectasis, chronic sinusitis, and situs inversus. This case report presents a 14‐year‐old girl from rural Bangladesh diagnosed with KS, who exhibited progressive respiratory ...
Nahid Afsar +4 more
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Aerobic exercise training in Kartagener's syndrome: case report. [PDF]
J Exerc Rehabil, 2019 Kartagener’s syndrome is a rare, autosomal recessive inherited disease, which is characterized by a triad of chronic sinusitis, bronchiectasis, and situs inversus.
Cakmak A +10 more
europepmc +2 more sources
Anesthetic Management of Dextrocardia with Situs Inversus for Caesarean Section- A Case Report [PDF]
Siriraj 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 +3 more sources
Kartagener’s Syndrome with Short Stature – A Rare Association [PDF]
JK ScienceKartagener’s syndrome [KS] is a rare, autosomal recessive disease comprising a triad of situs inversus, bronchiectasis and sinusitis. Usually, KS manifest in early childhood and the manifestations include chronic, thick, mucoid rhinorrhoea, recurrent ...
Thoyaj KJ, Chandrik Babu
doaj +1 more source
MGM Journal of Medical SciencesKartagener’s syndrome (KS) is a rare autosomal recessive genetic disorder primarily characterized by impaired ciliary function, leading to respiratory complications.
Nidhi Yadav +3 more
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Kartagener’s syndrome and psychotic disorder : a case report [PDF]
Eur PsychiatryIntroduction Kartagener’s syndrome, is a rare congenital malformation characterised by a triad : situs inversus, chronic sinusitis and bronchiectasis, and has rarely been associated with psychiatric manifestations.
Ilahi I +6 more
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Kartagener syndrome: Case report. [PDF]
, 2021 Kartagener’s syndrome is an autosomal recessive disease, characterized by primary ciliary dyskinesia, which consists of ciliated cell dysfunction. This is the cause of the manifestation of the respiratory symptomatology that presents this syndrome-cough,
Fajardo, German +3 more
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Kartagener’s Syndrome: A Classical Case [PDF]
, 2014 Background: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter in our clinical practice. Failure to recognize the specific cause of this condition may subject the patients to unnecessary and inappropriate treatment ...
Arunabha, DC +4 more
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Comparison of respiratory functions, muscle strength, and physical activity among children with primary ciliary dyskinesia with and without Kartagener’s syndrome and healthy controls [PDF]
, 2023 Introduction: Kartagener’s syndrome (KS), consisting of bronchiectasis, situs inversus totalis, and sinusitis, is a subtype of primary ciliary dyskinesia (PCD). The presence of KS may affect respiratory and physical functions.
Mutlu, Şeyma +3 more
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Live birth after Laser Assisted Viability Assessment (LAVA) to detect pentoxifylline resistant ejaculated immotile spermatozoa during ICSI in a couple with male Kartagener's syndrome. [PDF]
Reprod Biol Endocrinol, 2018 Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive disease with abnormalities in the structure of cilia, causing impairment of muco-ciliary clearance with respiratory tract infections, heterotaxia and abnormal sperm motility with male ...
Ozkavukcu S +3 more
europepmc +2 more sources