Other Names for this Disease
- Sneddon's syndrome
- Livedo reticularis and cerebrovascular accidents
- Cerebro-vascular lesions and livedo reticularis
- Ehrmann-Sneddon syndrome
- Livedo racemosa and cerebrovascular accidents
livedo reticularis (bluish net-like patterns of discoloration on the skin) and neurological abnormalities. Symptoms may include headache, dizziness, high blood pressure, heart disease, mini-strokes and/or stroke. Reduced blood flow to the brain may cause lesions to develop within the central nervous system. This can lead to reduced mental capacity, memory loss and other neurological symptoms. The exact cause of Sneddon syndrome is unknown. Some familial cases have been described. It has also been associated with obliterating vasculitis and antiphospholipid antibody syndrome.Sneddon syndrome is a progressive condition characterized by
Last updated: 2/22/2012
- Sneddon Syndrome. National Organization for Rare Disorders (NORD). 2002; http://rarediseases.org/rare-diseases/sneddon-syndrome/. Accessed 2/22/2012.
- Blanchet-Bardon C. Sneddon syndrome. Orphanet. 2002; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=820. Accessed 2/22/2012.
- Genetics Home Reference (GHR) contains information on Sneddon syndrome. This website is maintained by the National Library of Medicine.
- The National Organization for Rare Disorders (NORD) has a report for patients and families about this condition. NORD is a patient advocacy organization for individuals with rare diseases and the organizations that serve them.
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Sneddon syndrome. Click on the link to view a sample search on this topic.