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KCNJ2 gene spontaneous missense mutation in a child with Andersen-Tawil syndrome: a case report

Meiqi Feng1, Xi Wang1, Lingshan Hu1

  • 1Department of Endocrinology and Metabolism, Shandong Medical and Pharmaceutical University Hospital, Shandong Medical and Pharmaceutical University, Binzhou, Shandong, China.

Frontiers in Pediatrics
|October 27, 2026
PubMed
Abstract

Keywords:
Andersen-Tawil syndromeKCNJ2arrhythmiahypothyroidismmutationperiodic paralysis

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