Kartagener's syndrome - Open Access .click

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Kartagener's Syndrome in a Child: a Six year Follow-up.

Nigerian Journal of Paediatrics
Summary: A four-year old boy with Kartagener's syndrome is reported because of its rarity and being the first case to our knowledge, to be documented in Nigeria. There was situs inversus with visceroatrial concordance.
Ahmed H , Alhassan K , Amole AO
doaj

Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome. [PDF]

Asian J Androl, 2021
Huang C +6 more
europepmc +1 more source

Kartagener’s Syndrome with Short Stature – A Rare Association

JK Science
Kartagener’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

Successful Transjugular Percutaneous Atrial Septal Defect Closure in a Dextrocardia Patient with Kartagener's Syndrome, Situs Inversus, Interrupted Inferior Vena Cava, and Bilateral Superior Vena Cava. [PDF]