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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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Medknow Publications
2026-01-01
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| Seri Bilgileri: | Annals of Indian Academy of Neurology |
| Konular: | |
| Online Erişim: | https://journals.lww.com/10.4103/aian.aian_498_25 |
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