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Case Report

Delayed Diagnosed Atypical Case of Andersen-Tawil Syndrome

by
Ahmet Z. Burakgazi
Neuroscience Section, Department of Medicine, Virginia Tech Carilion School of Medicine, Roanoke, Virginia, USA
Neurol. Int. 2019, 11(2), 8180; https://doi.org/10.4081/ni.2019.8180
Submission received: 19 May 2019 / Revised: 19 May 2019 / Accepted: 11 June 2019 / Published: 18 June 2019

Abstract

Andersen-Tawil syndrome (ATS) is characterized by a triad of periodic paralysis, cardiac arrhythmias and distinctive dysmorphic features. Due to its rarity and high degree of clinical and phenotypic variability, a diagnosis of ATS can be very perplexing and challenging. Herein, an atypical case of ATS with a complicated presentation that caused an approximately 11-year delay in diagnosis is reported. The patient made a full recovery with acetazolamide after the diagnosis. The case and its management are presented with an updated literature review.
Keywords: Andersen-Tawil syndrome; Delayed diagnosed; literature review Andersen-Tawil syndrome; Delayed diagnosed; literature review

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MDPI and ACS Style

Burakgazi, A.Z. Delayed Diagnosed Atypical Case of Andersen-Tawil Syndrome. Neurol. Int. 2019, 11, 8180. https://doi.org/10.4081/ni.2019.8180

AMA Style

Burakgazi AZ. Delayed Diagnosed Atypical Case of Andersen-Tawil Syndrome. Neurology International. 2019; 11(2):8180. https://doi.org/10.4081/ni.2019.8180

Chicago/Turabian Style

Burakgazi, Ahmet Z. 2019. "Delayed Diagnosed Atypical Case of Andersen-Tawil Syndrome" Neurology International 11, no. 2: 8180. https://doi.org/10.4081/ni.2019.8180

APA Style

Burakgazi, A. Z. (2019). Delayed Diagnosed Atypical Case of Andersen-Tawil Syndrome. Neurology International, 11(2), 8180. https://doi.org/10.4081/ni.2019.8180

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