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Cutis Laxa
Topic Contents
Cutis Laxa Internationale

Cutis Laxa

Self Help Clearinghouse
This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.

Cutis Laxa Internationale

International. Founded 2001. Support group for those afflicted with any type of cutis laxa, a rare genetic disorder. Networking, promotes research and advocacy. Dues $55/yr. or L25/yr.
Write:
Cutis Laxa Internationale
35 route des Chaignes
17740 Sainte Marie de Re, France
Voice: 33 (0)5 46 55 00 59
Website: http://www.orpha.net/nestasso/cutislax
E-mail: mcjlboiteux@aol.com
Verified: 9/30/2008

The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information.

For additional information on self-help groups, please visit the American Self-Help Group Clearinghouse web site at http://www.mentalhelp.net/selfhelp

If you find information that is not current, please contact American Self-Help Group Clearinghouse at: admin@selfhelpgroups.org

Copyright © 2009 American Self-Help Group Clearinghouse. All rights reserved.

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