Case Report of Andersen–Tawil Syndrome: Rare Presentation of a Rare Disease

Andersen–Tawil syndrome (ATS) is a rare genetic disorder characterized by a triad of periodic paralysis, cardiac arrhythmias, and dysmorphic features, typically presenting in the first two decades of life. A 45-year-old man presented with acute lower motor neuron-type quadriparesis. He reported simi...

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Bibliografiske detaljer

Principais autores:	Himanshu Shakya, Shivangi Bhatnagar, Pratik Babel, Suman Kushwaha, Rajinder K Dhamija
Format:	Artigo
Sprog:	Inglês
Udgivet:	Wolters Kluwer Medknow Publications 2026-01-01
Serier:	Annals of Indian Academy of Neurology
Fag:	andersen-tawil syndrome periodic paralysis channelopathy kcnj2
Online adgang:	https://journals.lww.com/10.4103/aian.aian_498_25
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