Delayed diagnosed atypical case of Andersen-Tawil syndrome

dc.contributor.author	Burakgazi, Ahmet Z.	en
dc.date.accessioned	2019-07-24T17:19:13Z	en
dc.date.available	2019-07-24T17:19:13Z	en
dc.date.issued	2019	en
dc.description.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.	en
dc.format.extent	3 pages	en
dc.format.mimetype	application/pdf	en
dc.identifier.doi	https://doi.org/10.4081/ni.2019.8180	en
dc.identifier.uri	http://hdl.handle.net/10919/91971	en
dc.identifier.volume	11	en
dc.language.iso	en	en
dc.publisher	PAGEPress	en
dc.rights	Creative Commons Attribution Non-Commercial 4.0 International	en
dc.rights.uri	http://creativecommons.org/licenses/by-nc/4.0/	en
dc.subject	Andersen-Tawil syndrome	en
dc.subject	Delayed diagnosed	en
dc.subject	literature review	en
dc.title	Delayed diagnosed atypical case of Andersen-Tawil syndrome	en
dc.title.serial	Neurology International	en
dc.type	Article - Refereed	en
dc.type.dcmitype	Text	en

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