DISCINESIA CILIAR PRIMARIA PDF

La discinesia ciliar primaria es una enfermedad de origencongénito (herencia autosómica recesiva) que se caracterizapor una disfunción total o parcial de las . La prevalencia del síndrome de discinesia ciliar primaria (SDCP) en los Países Occidentales es de 1/ y entre los pacientes con bronquiectasias es del. Disease definition. Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower.

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No presente relato, quatro pacientes eram do sexo masculino.

Pediatrics, 23pp. Nasal brushing and measurement of ciliary beat frequency. Services on Demand Journal.

Primary ciliary dyskinesia

The immotile cilia syndrome: Regular clinical visits to monitor disease status are key. All the contents discinesja this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Archivos de Bronconeumologia http: January Pages The immotilia cilia syndrome: Are you a health professional able to prescribe or dispense drugs? Continuing navigation will be considered as acceptance of this use. Previous article Next article.

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Clinics in Chest Medicine, 9pp. J Med Genet ; Acta Otolaryngol Stockh ; Ciliary dyskinesia in the nose and the primadia sinuses. Reduced fertility or a history of ectopic pregnancies has been reported in affected women.

Acta Otorhinolaryngol Belg ; Geremek M, Witt M. Disease definition Primary ciliary dyskinesia PCD is a rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower respiratory tract disease.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Clinical description Affected patients develop signs of PCD at birth or within the first few months of life. It is a monthly Journal that publishes a total of 12 issues, which contain these types of articles to different extents.

Hospital Practice, 21pp. Mutations in around 30 different genes throughout the genome have been found to be causative.

Kartagener’s syndrome with motile spermatozoa. Ao exame apresentava hipocratismo digital, estertores bibasais e sibilos difusos. Os outros dois casos eram de pacientes ciliwr, do sexo feminino e sem filhos.

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Ciliary disorientation in patients with chronic upper respiratory tract inflammation. How to cite this article. Services on Demand Journal. The documents contained in this web site are presented for information purposes only.

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Etiology Pulmonary disease in PCD is related to defects in lung defense mechanisms due to abnormal ciliary structure and function with impaired mucociliary clearance. Situs inversus, bronchiectasis, and sinusitis and its relation to immotile cilia: J Submicrosc Dicsinesia ; Des anomalies ciliaires son-elles toujous presents dans le syndrome de Kartagener?.

Update of an Orphan Disease.

Berl Klin Wochenschr ; A congenital ciliary abnormality as an etiologic factor in chronic airway infections and male sterility. Ciliary disorientation alone as a cause of primary ciliary dyskinesia. Si continua navegando, consideramos que acepta su uso.

Primary ciliary dyskinesia: considerations regarding six cases of Kartagener syndrome

To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. J Pediatr Rio de J. Inherited factors in diffuse bronchiectasis in the adult: