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Contrary to developed countries, the CIA still pose a big diagnostical and therapeutical problem in developing countries. Our study has been done to evaluate the work done. Our aim is to study the epidemiological, diagnostical and take over of the CIA in Togo. It is about retrospective study of 41 files of the children less than 15 years old, porters of the CIA registered at the TDH from January to December The clinical, paraclinical, therapeutical and evolutive perimeters have been studied and the treatment of results have been done by computer. The CIA represents

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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. An extremely rare genetic congenital heart disease characterized by the presence of atrial septal defect, mostly of the ostium secundum type, associated with conduction anomalies like atrioventricular block, atrial fibrillation or right bundle branch block.

Other search option s Alphabetical list. Suggest an update. Summary and related texts. Related genes. Clinical signs. Check this box if you wish to receive a copy of your message. Disease definition An extremely rare genetic congenital heart disease characterized by the presence of atrial septal defect, mostly of the ostium secundum type, associated with conduction anomalies like atrioventricular block, atrial fibrillation or right bundle branch block.

Detailed information Professionals Summary information Greek , pdf Russian , pdf. Additional information Further information on this disease Classification s 4 Gene s 1 Clinical signs and symptoms Other website s 1. Health care resources for this disease Expert centres Diagnostic tests 36 Patient organisations 45 Orphan designation s and orphan drug s 0. Specialised Social Services Eurordis directory. The documents contained in this web site are presented for information purposes only.

The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

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Liste des principales cardiopathies congénitales adultes

Background: Concerns remain that minimally invasive atrial septal defect ASD repair may compromise patient outcomes. We compared clinical outcomes of adult patients undergoing ASD repair via a minimally invasive endoscopic approach versus a "gold standard" sternotomy. Methods: We retrospectively reviewed the clinical outcomes of consecutive patients who underwent ASD patch repair at our institution between and There were no significant differences in any postoperative complications or blood product requirements. No patients in the MT group suffered stroke, retrograde aortic dissection or leg ischemia. Mean intensive care unit MT 1. Conclusion: Repair of ostium secundum and sinus venosus ASD can be performed safely via MT endoscopic approach with similar outcomes as sternotomy.

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These images are a random sampling from a Bing search on the term "Atrial Septal Defect. Search Bing for all related images. Started in , this collection now contains interlinked topic pages divided into a tree of 31 specialty books and chapters. Content is updated monthly with systematic literature reviews and conferences. Although access to this website is not restricted, the information found here is intended for use by medical providers.

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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. An extremely rare genetic congenital heart disease characterized by the presence of atrial septal defect, mostly of the ostium secundum type, associated with conduction anomalies like atrioventricular block, atrial fibrillation or right bundle branch block.

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