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Welcome to our homepage!

Cogan-I-syndrome is a rare disease which is unknown to many people. Therefore, our registered association,
Cogan-I-Syndrome Self-help Germany, aims to promote comprehensive information on this disease.
We try to continuously update the information published on this web site according to the current state of
scientific research.


Scientific supervision in the preparation of this website was received from:

Prof.  Dr.  W. J. Mann
Director, Ear Nose and Throat Clinic, University Clinics, Johannes Gutenberg-University Mainz, Germany
Langenbeckstr. 1, D 55101 Mainz

Cogan-I-Syndrome Self-Help Germany (CSS Deutschland e.V.) offers advice and information on this
disease and its treatment options.  

We promote the exchange between individual patients and represent the interests of all patients suffering
from Cogan-I-syndrome especially with health institutions and authorities. Further aims are to improve
the information on preventative and therapeutic options for people suffering from Cogan-I-syndrome
and to increase public awareness of this rare disease.

Contact:

Ute Jung (chairperson) Wilhelmstraße 45 56584 Anhausen Tel.: 02639/323 Fax: 02639/961734 E-Mail: ute.jung@cogan-syndrom.com www.das-cogan-syndrom.de	Barbara Anton (vice chairperson) Mittlerer Flurweg 49 55543 Bad Kreuznach Tel. : 0671/2244102 Fax: 0671/2244422 E-Mail: barbara.anton@freenet.de www.das-cogan-syndrom.de

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Articles of Assotiation CSS Deutschland e.V.                                   Membership application CSS e.V.


Our work is supported by donations which are most welcome.

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