Results 21 to 30 of about 2,234 (198)

Kartagener syndrome: A review of three cases

Sahel Medical Journal, 2015
Kartagener's syndrome (KS) is an autosomal recessive subgroup of primary ciliary dyskinesia (PCD) which presents as sinusitis, bronchiectasis, and dextrocardia .The deficit in the coordination of ciliary motion results in mucus retention and recurrent ...
Avadhesh Kumar, Ajay Kumar Verma, Anand Kumar, Prashant Yadav, Ankit Bhatia, Saurabh Pahuja, Surya Kant   +6 more
doaj   +2 more sources

Kartagener′s syndrome

Medical Journal of Dr. D.Y. Patil University, 2012
Bronchiectasis may have varied etiologies. In patients presenting in middle or old age with bronchiectasis, congenital and hereditary causes of bronchiectasis are not commonly encountered. In majority of adult patients, bronchiectasis follows necrotizing
Pradip V Potdar, Mitali M Nayak, Aushutosh Chitnis   +2 more
doaj   +2 more sources

Síndroma de Kartagener

Revista Portuguesa de Pneumologia, 2005
Resumo: Apresentouse para atendimento uma mulher de 48 anos, branca, natural e procedente de Uberaba-MG, com quadro de dispneia em repouso, febre, tosse produtiva, escarro esverdeado e dor torácica ventilatório-dependente há 3 dias.
Kattia Cristina Naves, João Paulo Vieira dos Santos, José Henrique Santana, Gesner Pereira Lopes   +3 more
doaj   +2 more sources

Kartagener syndrome

Dentomaxillofacial Radiology, 2006
Kartagener syndrome (KS), an autosomal recessively inherited disease, is characterized by the triad of situs inversus, bronchiectasis and sinusitis. This disorder affects the activity of proteins important to the movement of cilia, especially in the respiratory tract and the spermatozoa, developing a series of systemic alterations, which can be ...
M S, Casanova, F M, Tuji, H J, Yoo, F, Haiter-Neto   +3 more
openaire   +3 more sources

International Collaboration in Primary Ciliary Dyskinesia. [PDF]

Pediatr Pulmonol
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 ...
Pennekamp P, Manion M, Omran H.
europepmc   +2 more sources

Research Hotspots and Trends in Ciliopathies: A Bibliometric and Visualization Analysis. [PDF]

Biomed Res Int
Purpose This study conducted a comprehensive bibliometric analysis of research hotspots and development trends in ciliopathies to provide an overview of the global research landscape. Methods The study retrieved relevant literature on ciliopathies from the Web of Science Core Collection up to July 27, 2024.
Dong Q, Zhu J, Liu J, Xu H.
europepmc   +2 more sources

Kartagener's syndrome presenting with secondary spontaneous pneumothorax: A rare case report

Journal of Association of Pulmonologist of Tamil Nadu, 2022
Kartagener's syndrome (KS) is a part of a larger family of diseases classified as primary ciliary dyskinesia (PCD). The triad of KS consists of bronchiectasis, chronic sinusitis, and situs inversus, which is likely underdiagnosed, as a limited amount of ...
Niranjan Prabhakar, R Anand, Preetha Ramesh   +2 more
doaj   +1 more source

Zero-Fluoroscopy Radiofrequency Ablation of a Right Ventricular Outflow Tract PVC in a Patient With Situs Inversus Totalis: When Precision Matters. [PDF]

Case Rep Cardiol
Background Congenital cardiac anomalies present unique challenges for adult cardiac electrophysiologists, particularly when attempting complex ablation procedures. Case Summary We report the case of a 60‐year‐old male with situs inversus totalis who presented with symptomatic, high‐burden premature ventricular complexes (PVCs) refractory to medical ...
Sanhueza E, Hanson M, Neira V, Chacko S, Enriquez A, Oli R, Saramago M, Burak C.   +7 more
europepmc   +2 more sources

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, Cárcamo, Gloria, Rivera, Velia, Flores, Brigitte   +3 more
core   +2 more sources

KARTAGENER SYNDROME: A CASE REPORT [PDF]

, 2018
Kartagener syndrome is a rare genetic disorder which includes a triad of bronchiectasis, chronic sinusitis, and situs inversus. Primary ciliary dyskinesia (PCD) can be one of the causes of the above symptoms in this syndrome.
Najafi, Samane, Eshghizadeh, Maryam, Mohammadpour, Ali   +2 more
core   +3 more sources