Rare Diseases on the Internet: An Assessment of the Quality of Online Information.
Frédéric PauerSvenja LitzkendorfJens GöbelHolger StorfJan ZeidlerJ-Matthias Graf von der SchulenburgPublished in: Journal of medical Internet research (2017)
Overall, the quality of information on the Internet about rare diseases is low. Quality certificates are rarely used and important quality criteria are often not fulfilled completely. Additionally, some information categories are underrepresented (eg, information about psychosocial counseling, social-legal advice, and family planning). Nevertheless, due to the high amount of information provided by support groups, this study shows that these are extremely valuable sources of information for patients suffering from a rare disease and their relatives.