BICUSPIDIE AORTIQUE PDF

BICUSPIDIE AORTIQUE PDF

La bicuspidie de la valve aortique est la pathologie congénitale la plus fréquente, touchant selon les séries prospectives 0,5 à 2% de la population générale. Disease definition. Familial bicuspid aortic valve is a rare, genetic, aortic malformation defined as a presence of abnormal two-leaflet aortic. Summary. An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional.

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Browsing AD1: Département des Sciences Médicales by Subject “Bicuspidie aortique”

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bicuspidie aortique

Previous Article Bicuspidie aortique R. The material aaortique 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. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.

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Summary and related texts. Familial bicuspid aortic valve is a rare, genetic, aortic malformation defined as a presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives.

Browsing AD1: Département des Sciences Médicales by Subject “Bicuspidie aortique”

Check this box if you wish to receive a copy of your message. Summary Bicuspiie Orphanet summary for this disease is currently under development. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.

Summary and related texts. The documents contained in this web site are presented for information purposes only. Disease definition Familial bicuspid aortic valve is a rare, genetic, aortic malformation defined as a presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives.

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Diagnostic et classification anatomique. You can move this window by clicking on the headline. Additional information Further information on this disease Classification s 0 Gene s 0 Other website s 0. You may thus request bicuspodie your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.

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Health care resources for this disease Expert centres 1 Diagnostic tests 2 Patient organisations 0 Orphan drug s 0.

If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Additional information Further information on this disease Classification s 5 Gene s 4 Clinical signs and symptoms Other website s 0. Contact Help Who are we? Specialised Social Services Eurordis directory. Only comments written in English can be processed. Journal page Archives Contents list. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Personal information regarding our website’s visitors, including their identity, is confidential.

However, other data related aoftique the disease are accessible from the Additional Information menu located at the bottom of this page.

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