{"id":1285,"date":"2018-01-19T13:06:48","date_gmt":"2018-01-19T13:06:48","guid":{"rendered":"https:\/\/belgianfapa.anmdev.be\/?page_id=1285"},"modified":"2025-04-20T09:21:46","modified_gmt":"2025-04-20T07:21:46","slug":"a-propos-de-fapa","status":"publish","type":"page","link":"https:\/\/belgianfapa.be\/fr\/a-propos-de-fapa\/","title":{"rendered":"A propos de FAPA"},"content":{"rendered":"

FAPA est une asbl qui a \u00e9t\u00e9 cr\u00e9\u00e9e en 1993. Ses membres fondateurs repr\u00e9sentent les 7 centres universitaires du pays et toutes les disciplines m\u00e9dicales directement concern\u00e9es par la polypose ad\u00e9nomateuse familiale. Depuis sa cr\u00e9ation, l\u2019association a \u00e9largi ses contacts \u00e0 de nombreux centres hospitaliers non universitaires.<\/p>\n

Des professionnel-le-s sont actif-ve-s au sein de l’organisation depuis 1996. En 2012, l’action de la FAPA a \u00e9t\u00e9 \u00e9tendue aux familles atteintes du syndrome de Lynch (HNPCC = hereditary non-polyposis colorectal cancer).<\/p>\n

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\n Rapport annuel 2023<\/a>\n <\/div>\n
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\n Rapport annuel 2018<\/a>\n <\/div>\n
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\n Rapport annuel 2017<\/a>\n <\/div>\n
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