Other Names for this Disease
- Andersen cardiodysrhythmic periodic paralysis
- Andersen syndrome
- Long QT syndrome 7
- Periodic paralysis, potassium-sensitive cardiodysrhythmic type
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
long QT syndrome and is also considered a rare form of periodic paralysis. It causes episodes of muscle weakness, changes in heart rhythm (arrhythmia), and developmental abnormalities. Physical abnormalities associated with this condition typically affect the head, face, and limbs. There are two different types of Andersen-Tawil syndrome. Type 1 is caused by changes in the KCNJ2 gene, while the cause of type 2 is not yet known. Andersen-Tawil syndrome is inherited in an autosomal dominant pattern.Andersen-Tawil syndrome is a type of
Last updated: 10/11/2011
- Andersen-Tawil syndrome. Genetics Home Reference. April 2006; http://ghr.nlm.nih.gov/condition/andersen-tawil-syndrome. Accessed 10/11/2011.
Your Questions Answeredby the Genetic and Rare Diseases Information Center
Please contact us with your questions about Andersen-Tawil syndrome. We will answer your question and update these pages with new resources and information.
- Genetics Home Reference (GHR) contains information on Andersen-Tawil syndrome. This website is maintained by the National Library of Medicine.
- The National Heart, Lung, and Blood Institute (NHLBI) provides leadership for a national program in diseases of the heart, blood vessels, lung, and blood; blood resources; and sleep disorders. Since October 1997, the NHLBI has also had administrative responsibility for the NIH Woman's Health Initiative. Click on the link to view information on this topic.
- Medscape Reference provides information on this topic. Click on the link to view this information. You may need to register to view the medical textbook, but registration is free.
- MeSH® (Medical Subject Headings) is a terminology tool used by the National Library of Medicine. Click on the link to view information on this topic.
- The 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 Andersen-Tawil syndrome. Click on the link to view a sample search on this topic.
- Identification and Treatment of Sudden Death Conditions in Young Patients. A presentation by David Bradley, M.D., Director, Pediatric Heart Rhythm Service, CS Mott Children's Hospital. Assoicate Professor, Department of Pediatrics and Communicable Diseases, University of Michigan.