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Tag der Seltenen Erkrankungen: "Internet-Arzt" Dr. med. Johannes Wimmer klärt über das "hereditäre Angioödem" (HAE) auf

Betroffene leiden an immer wiederkehrenden Schwellungen am gesamten Körper und stellen Ärzte damit oft vor ein Rätsel

(PresseBox) (Marburg, )
In Deutschland leiden 4 Mio. Menschen an einer seltenen Erkrankung. Was sie gemeinsam haben: Aufgrund des geringen Bekanntheitsgrads ihrer Erkrankung durchleben viele von ihnen einen zum Teil jahrelangen Leidensweg bis zur richtigen Diagnose. Um auf diese Erkrankungen und die Schicksale der Betroffenen aufmerksam zu machen, findet jedes Jahr am 28. oder 29. Februar weltweit der „Tag der Seltenen Erkrankungen" statt. Anlässlich des diesjährigen Aktionstags thematisiert der aus Internet, TV und Print bekannte Mediziner Dr. med. Johannes Wimmer in seinem aktuellen Video das „hereditäre Angioödem". Anschaulich beleuchtet er die Ursache, die Symptome und die guten Behandlungsmöglichkeiten der seltenen Erkrankung und motiviert nvs Khuyrqht aux Pzfcqhuxmh.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.