Results 91 to 100 of about 2,234 (198)

Síndrome de kartagener reporte de caso

, 2014
Kartagener syndrome is an autosomic recessive hereditary disease characterized of primary ciliary dyskinesia, chronic cough, chronic sinusitis, infertility, situs inversus, and bronchiectasis.
Claudia Carrillo, María, Cano, Rodolfo, Guerra Lopez, Foris, Luna, Karen   +3 more
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APLICAÇÃO DE UM PROTOCOLO FISIOTERAPÊUTICO NA SÍNDROME DE KARTAGENER: ESTUDO DE CASO

Arquivos de Ciências da Saúde da UNIPAR, 2011
A Síndrome Kartagener é uma doença autossômica recessiva rara que se caracteriza por situs inversus e discinesia ciliar, Além disso essa enfermidade pode desencadear sinusite paranasal e bronquiectasia.
Bruna Gallo da Silva, Andréia Regina Martins, Ivete Alonso Bredda Saad   +2 more
doaj  

Síndrome de Kartagener: A propósito de un caso

, 2022
Introduction: Kartagener syndrome is a rare autosomal hereditary pathology characterized by the triad situs inversus, sinusitis and bronchiectasis, it appears at birth, childhood or adulthood. Objective: To describe the nursing care process carried out
Paccha Tamay, Carmen Liliana, Macas Macas, Rosa Patricia, Arias Pintado, Diana Ivonne   +2 more
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Síndrome de Kartagener, reporte de caso

Revista Médica Hondureña
Introduction: Kartagener Syndrome is a clinical variant of primary ciliary dyskinesia It is a rare autosomal recessive disease, one in every 32,000 births, characterized by a triad of bronchiectasis, chronic sinusitis and situs ...
Suyapa Sosa Ferrari, Luisa Rodríguez, Gerardo Mejía, Javier Sánchez   +3 more
doaj   +1 more source

Síndrome de Kartagener

, 2019
Kartagener syndrome is an autosomic recessive hereditary disease characterized of primary ciliary dyskinesia, chro- nic cough, chronic sinusitis, infertility, situs inversus, and bronchiectasis.
Orozco, Karen Luna, Cano, Rodolfo, Guerra Lopez, Foris, Carrillo, María Claudia   +3 more
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Kartagener's Syndrome [PDF]

BMJ, 1949
openaire   +2 more sources

Kartagener sendromu: Bir olgu

, 2009
Kartagener sendromu, otozomal resesif (OR) geçişli, bronşektazi, situs inversus, sinüzit, kronik üst ve alt solunum yolu enfeksiyonları ve bronşiektazi ile karakterizedir. Primer silier diskinezi 20000 canlı doğumda bir görülen nadir bir durumdur.
Öztürk, Esma, Dursunoğlu, Neşe, Özkurt, Sibel   +2 more
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Kartagener′s syndrome in a fertile male - An uncommon variant

Lung India, 2006
Primary ciliary dyskinesia, with Kartagener′s syndrome as one of the subsets, is an autosomal recessive disorder with significant genetic heterogeneity.
Barthwal M
doaj  

Persistent cough and situs inversus in a middle‐aged female

Respirology Case Reports
Key message Kartagener syndrome, a rare genetic disorder, can present in adults with persistent respiratory symptoms and radiological changes, such as bronchiectasis and situs inversus.
Besharat Rahimi, Ghazal Roostaei, Hossein Kazemizadeh, Maryam Edalatifard, Niloofar Khoshnam‐Rad   +4 more
doaj   +1 more source

Scholars Journal of Medical Case Reports ISSN 2347-9507 (Print) A Case Report of Kartagener Syndrome

, 2020
: Kartagener syndrome/Primary ciliary dyskinesia (PCD) is a rare ciliopathic autosomal recessive genetic disorder that causes defects in the action of cilia lining the respiratory tract (both lower and upper, sinuses, eustachian tube, middle ear) and ...
Dr Priyanshu Mathur, Dr Rajesh Kumar, Dr Ashok Gupta, Dr Manish Sharma, Dr Manisha Garg, Dr Manjunath S Pandit   +5 more
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