Alport Foundation of Australia

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This is the website of the US Alport Foundation. It is linked to the Alport Syndrome Treatments

and Outcomes Registry (ASTOR) and has contact details for genetic testing laboratories

worldwide and for kidney and skin immunohistochemistry in North America.

United Kingdom–based patient support group that provides information for families

affected by Alport syndrome and brings together professionals with a particular

interest in the condition.

ASTOR is a voluntary international patient registry established at the University of

Minnesota that aims to provide patients and families with the most current information

about Alport syndrome. Information from this registry will be used to design future


Alport Orphanet is a mainly European-centric site that describes the disease classifications;

lists recent medical publications; links to other relevant websites; and gives contact

details for expert treating centers, diagnostic testing laboratories, patient support

groups, funding groups, research projects, clinical trials and registries, biobanks and


These curated COL4A5 mutation databases are hosted by the LOVD and ARUP Laboratories.

This useful and comprehensive overview of Alport syndrome from NCBI provides specific genetic information clearly described for each form of inheritance.

This is a voluntary international patient registry established at the University of Goettingen,

Germany. PRO-TECT

This website has information about the phase III, multicenter, randomized, double-blind, placebo-controlled trial to investigate the optimal timing of ACE inhibitor therapy and its safety in pediatric patients with early-stage disease.

ASTOR, Alport Syndrome Treatments and Outcomes Registry; LOVD, Leiden Open Variation Database; NCBI, National Center for Biomedical Information

Email if you know of any other helpful websites to add to this list