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Other Names for this Disease
- Andersen cardiodysrhythmic periodic paralysis
- Andersen syndrome
- Long QT syndrome 7
- Periodic paralysis, potassium-sensitive cardiodysrhythmic type
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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.
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- Genetics Home Reference (GHR) contains information on Andersen-Tawil syndrome. This website is maintained by the National Library of Medicine.
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- The Online Mendelian Inheritance in Man (OMIM) is an 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.
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- 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.