Disclaimer

The Alport Syndrome Foundation (ASF) provides this website for educational purposes to people interested in Alport Syndrome. ASF does not provide medical advice or services, or specifically endorse any individual or clinician in the diagnosis and treatment of this disease. Health-related topics found on this website should not be used for diagnostic purposes or be substituted for medical advice. As with any new or ongoing treatment, always consult your physician.

ASF assumes no responsibility or liability for any consequence resulting directly or indirectly from any action or inaction you take based on or made in reliance on the information, services, or material on or linked to this site.

Since medical developments change frequently, this site may contain outdated material. While ASF makes reasonable efforts to present current and accurate information, no guarantee of any kind is made. ASF is not liable for any damage or loss related to the accuracy, completeness or timeliness of any information contained on this site.

Links:
Any links or external websites are provided as a courtesy only. ASF has no responsibility for the accuracy or content of information provided by these sites nor should they be construed as an endorsement by ASF of the content or views of the linked materials.

Social Media:
Opinions expressed by contributors through discussion on Social Media, including but not limited to Facebook and Twitter, are not necessarily those of ASF.

Contact:
The names and contact information on this website are published to facilitate contact among those listed for ASF purposes only. These names and contact information are not intended for any commercial purposes.

Downloads:
Individuals may download useful material from this website for non-commercial use only. For reprint permission, please contact ASF at info@alportsyndrome.org.

Copyright:
The information on this website is protected under the copyright laws of the United States and other countries. All information contained within this website is the property of the Alport Syndrome Foundation.

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