Andersen-Tawil syndrome history and symptoms: Difference between revisions

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{{Andersen-Tawil syndrome}}
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==Overview==
==Overview==
*[[Seizures]] - due to [[oxygen]] deprivation that occurs during [[arrhythmia]].
*The most common symptoms of  [[Andersen-Tawil syndrome|Andersen-Tawil Syndrome]] include periodic paralysis, ventricular arrhythmias, [[syncope]], [[muscular weakness]], developmental abnormalities, [[sudden cardiac death]] and [[Seizure|seizures]].
*[[Fainting]] - fainting or [[syncope]] is the most common symptom LQTS.
* A prodrome may occur before losing consciousness, which may consist of [[lightheadedness]], heart [[palpitations]], [[blurred vision]] or [[weakness]].
*[[Sudden death]] - a fatal [[arrhythmia]] that is not quickly intervened on, may cause sudden death.
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{{WikiDoc Sources}}
{{WikiDoc Sources}}
[[Category:Electrophysiology]]
[[Category:Electrophysiology]]
[[Category:Disease]]
[[Category:Rare Disease]]
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Cardiology]]
[[Category:Cardiology]]

Latest revision as of 15:08, 17 February 2020

Andersen-Tawil syndrome Microchapters

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Overview

Historical Perspective

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Pathophysiology

Differentiating Andersen-Tawil syndrome from other Diseases

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History and Symptoms

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]

Overview

History and Symptoms

History

Patients with Andersen-Tawil Syndrome may have a positive history of:

Common Symptoms

Common symptoms of Andersen-Tawil Syndrome include:[1][2]

Less Common Symptoms

Less common symptoms of Andersen-Tawil Syndrome include:

References

  1. Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A; et al. (2002). "Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)". J Clin Invest. 110 (3): 381–8. doi:10.1172/JCI15183. PMC 151085. PMID 12163457.
  2. Sansone V, Griggs RC, Meola G, Ptácek LJ, Barohn R, Iannaccone S; et al. (1997). "Andersen's syndrome: a distinct periodic paralysis". Ann Neurol. 42 (3): 305–12. doi:10.1002/ana.410420306. PMID 9307251.


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