Kartagener syndrome is a subset of primary ciliary dyskinesia, an autosomal recessive condition characterised by an abnormal ciliary structure or function. Kartagener syndrome, current data on a classical disease. Case report. Keywords: Kartagener Syndrome; Primary. Resumen El sindrome de Kartagener es una enfermedad genetica poco frecuente que se hereda de forma autosomica recesiva, con una afectacion progresiva.

Author: Nar Kazigami
Country: France
Language: English (Spanish)
Genre: Relationship
Published (Last): 2 January 2012
Pages: 127
PDF File Size: 9.39 Mb
ePub File Size: 5.33 Mb
ISBN: 344-9-68213-785-8
Downloads: 34846
Price: Free* [*Free Regsitration Required]
Uploader: Arashigrel

Loading Stack – 0 images remaining. Case 1 Case 1. View in Source Cite this paper. En el presente articulo se describe la compleja interrelacion entre la variacion genetica y un tratamiento inespecifico apropiado del sindrome. For some authors, laterality is determined even during oogenesis when the chromatids separate; in any case, their clinical kartagenfr is not clear.

Kartagener syndrome | Radiology Reference Article |

Am Rev Respir Dis,pp. D utta M, Sarma J. More on Kartagener’s syndrome and the contributions of Afzelius and A. Manes Kartagener 1who described the presence of paranasal sinusitis in patients in association with situs inversus and kagtagener observed by Siewert in Paranasal sinus tomography with thickening of the mucosal lining, partially occupied by a soft tissue density mass.

  CARCASSONNE RULEBOOK PDF

Ann Allergy, 73pp. You can also scroll through stacks with your kartagenre wheel or the keyboard arrow keys. CT provides good anatomical detail of the specific condition, while MRI can be useful to assess patients with cardiac abnormalities. Short Cases Respir Med, 2pp. Inadequate sweeping of pulmonary secretions causes bronchial dilatations or bronchiectasis that are observed as tubular opacities or ovoids of variable sizes in chest x-ray, a less sensitive method for its detection with respect to HRCT.

New development in the diagnosis of Enermedad syndrome. Simple tomography showing that the liver H is to the left of the midline and the spleen B to the right.

Cilia, primary ciliary dyskinesia and molecular genetics. No images or control laboratory exams were made. Genetic diagnosis is available and multi-gene panels include most of the genes related to PKD.

A simple enferedad documented pulmonary bronchiectasis, as well as liver on the left side Figure 4leading to suspect KS; this was confirmed with findings of chronic sinusitis in paranasal sinus tomography. En el presente informe se describe un caso clinico del sindrome en una mujer de 25 anos de edad. Immotile cilia syndrome in persons with and without Kartagener’s syndrome.

  CARTEA REGALA DE BUCATE A PRINCIPESEI MARGARETA PDF

BodoutchianHitender JainTania Velez. Despues de 7 anos, se obtuvieron resultados satisfactorios del tratamiento: Hospital Universitario La Paz. This article addresses the general aspects pathophysiology, embryology, clinical presentation and prognosis of the Kartagener syndrome KS.

Case reports

The differential diagnoses that should be considered depend on the moment of symptom onset: Chang 53 Estimated H-index: Edit article Share article View revision history. Consequences of ciliary dysfunction.

Beitr Klin Tuberk Spezif Tuberkuloseforschung. About Blog Go ad-free. Zur Pathogenese der Bronchiektasien. You can change the settings or obtain more information by clicking here.

There was a problem providing the content you requested

Altered dynein in animal models, known as left-right dynein and encoded by gene IV inversus viscerumcauses situs ambiguus. Situs inversus totalis – a case report. The Kartagener syndrome KS comprises a triad of situs inversus, bronchiectasis and paranasal sinusitis, which is named after Dr.