Bronchiectases in Children: Overview of Current Clinical Guidelines
Педиатрическая фармакология, 2017 The article is devoted to bronchiectases issue in children and reflects the most actual approaches to the diagnosis and management of patients with this pathology.
A. A. Baranov +11 more
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Kartagener's syndrome presented with nasal obstruction: A case report
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014 The nasal polyposis is a chronic inflammatory process of the nasal mucosa. Although it is rare in children, there may be also association with cystic fibrosis and primary ciliary dyskinesia.
Suna Asilsoy, Buket Kilicaslan, Cem Ozer
doaj
An unusual case of Kartagener's syndrome with fertility
Current Medical IssuesSitus inversus, chronic sinusitis, and bronchiectasis together make up the trinity that characterize the uncommon autosomal recessive genetic ciliary condition known as Kartagener's syndrome. The fundamental issue is the improper movement of cilia, which
Nithin Thomas +3 more
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Familial Kartageners Syndrome: A Case Report [PDF]
, 2014 In recurrent lower respiratory tract infections the cause may be either general impairment of immune mechanism, abnormalities of mucus or abnormalities of cilia.We report a case where the patient was having recurrent lower and upper respiratory tract ...
CHO, NASEER +4 more
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Prevalence of the metabolic syndrome in Chinese adolescents [PDF]
, 2008 Since national figures on the occurrence of metabolic syndrome among Chinese adolescents are lacking, this study aims to estimate its prevalence and distribution among Chinese youngsters.
Yang, X. +6 more
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SITUS INVERSUS TOTALIS ASSOCIATED WITH SUBAORTIC STENOSIS, RESTRICTIVE VENTRICULAR SEPTAL DEFECT AND TRICUSPID DYSPLASIA IN AN ADULT DOG [PDF]
, 2011 A rare association between situs inversus totalis (SIT), restrictive ventricular septal defect, severe subaortic stenosis, and tricuspid dysplasia was observed in an adult mixed-breed dog.
A. Di Loria +4 more
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Unveiling Kartagener’s Syndrome in a Young Male: A Case Report [PDF]
Journal of Clinical and Diagnostic ResearchKartagener'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
New Treatments Are Urgently Needed for Patients With All Primary Ciliary Dyskinesia Genotypes
Pediatric Pulmonology, Volume 60, Issue 11, November 2025.
Benjamin Gaston +10 more
wiley +1 more source
EFFICIENCY OF HYPERTONIC SOLUTION INHALATION IN CHILDREN WITH BRONCHITIS AND BRONCHIOLITIS
Вопросы современной педиатрии, 2014 Background: Chronic bronchitis and bronchiolitis in children with congenital malformation are often characterized by the severe course of disease. The efficiency of treatment of those conditions can be increased through addition of sodium chloride (NaCl),
O. I. Simonova +2 more
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Primary ciliary dyskinesia: current state of the art
, 2007 Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical form presents with upper and lower respiratory tract infection, and mirror image arrangement in around 50% cases.
Hall, Pippa +10 more
core +1 more source