A Rare Case of Anderson Tawil Syndrome

Andersen Tawil Syndrome (ATS) is a rare disorder, the prevalence of which is one in a million. We present case of a 37-year-old female with a long-standing history of periodic paralysis, and ventricular arrhythmias. She presented with generalized weakness which resolved with potassium supplementatio...

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Veröffentlicht in:Frontiers in Medical Case Reports 2023, Vol.4 (3)
Hauptverfasser: Nagpal, Sagar, C. Pokhriyal, Sindhu, Bhandari, Pooja, Parvez, Mohammad Amaan, Dalbah, Rami, Patel, Suyog, C. Gottipati, Keerthana
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Sprache:eng
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Zusammenfassung:Andersen Tawil Syndrome (ATS) is a rare disorder, the prevalence of which is one in a million. We present case of a 37-year-old female with a long-standing history of periodic paralysis, and ventricular arrhythmias. She presented with generalized weakness which resolved with potassium supplementation. Genetic workup revealed KCNJ2 mutation.
ISSN:2582-8142
2582-8142
DOI:10.47746/FMCR.2023.4301