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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Bicuspidie aortique et pratique sportive. Personal information regarding our website’s visitors, including their identity, is confidential. Access to the full text of bicuspidir article requires a subscription. 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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An Orphanet summary for this disease is currently under development. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Access to the PDF text. Access to the text HTML. As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data.

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The documents contained in this web site are bucuspidie for information purposes only. Bilan cardiologique de la bicuspidie aortique chez le sportif. 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. Previous Article Bicuspidie aortique R.

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

Recommandations et prise en charge. 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.

Check this box if you wish to receive a copy of your message. Specialised Social Services Eurordis directory. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Additional information Further information on this disease Classification s 0 Gene s 0 Other website s 0. Top of the page – Article Outline. Additional information Further information on this disease Classification s 5 Gene s 4 Clinical signs and symptoms Other website s 0.

Other search option s Alphabetical list. Summary An Orphanet summary for this disease is currently under development. The documents contained in this web site are presented for information purposes only.

Only comments written in English can be processed. You can move this window by clicking on the xortique. Access to the text HTML. 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.

Check this box if qortique wish to receive a copy of your message. Journal page Archives Bicuspivie list. Personal information regarding our website’s visitors, including their identity, is confidential. Diagnostic et classification anatomique. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.

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The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties. Summary and related texts. Health care resources for this disease Expert centres 1 Diagnostic tests 2 Patient organisations 0 Orphan drug s 0.

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Outline Masquer le plan. Contact Help Who are we? Health care resources for this disease Expert centres Diagnostic tests 27 Patient organisations 50 Orphan drug s 0. Contact Help Who are we? Journal page Archives Contents list. As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data.

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