Andersen-Tawil syndrome overview: Difference between revisions
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==Overview== | ==Overview== | ||
Andersen-Tawil syndrome is a form of [[long QT syndrome]]. It is a rare genetic disorder, and is inherited in an [[autosomal dominant]] pattern and has characteristic features of episodes of [[paralysis]], [[ventricular arrhythmia]], and [[dysmorphic]] features such as [[hypertelorism]], [[micrognathia]], and low set ears. Patients with Andersen-Tawil syndrome usually present in childhood with spontaneous attacks of [[paralysis]] which may be associated with normal, high, or low potassium levels. | Andersen-Tawil syndrome is a form of [[long QT syndrome]]. It is a rare genetic disorder, and is inherited in an [[autosomal dominant]] pattern and has characteristic features of episodes of [[paralysis]], [[ventricular arrhythmia]], and [[dysmorphic]] features such as [[hypertelorism]], [[micrognathia]], and low set ears. Patients with Andersen-Tawil syndrome usually present in childhood with spontaneous attacks of [[paralysis]] which may be associated with normal, high, or low potassium levels. | ||
==References== | ==References== | ||
Revision as of 20:49, 24 February 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Andersen-Tawil syndrome is a form of long QT syndrome. It is a rare genetic disorder, and is inherited in an autosomal dominant pattern and has characteristic features of episodes of paralysis, ventricular arrhythmia, and dysmorphic features such as hypertelorism, micrognathia, and low set ears. Patients with Andersen-Tawil syndrome usually present in childhood with spontaneous attacks of paralysis which may be associated with normal, high, or low potassium levels.