Neuromuscular tetanic hyperexcitability syndrome associated to a heterozygous Kv1.1 N255D mutation with normal serum magnesium levels

Francesca Bianchi, Costanza Simoncini, Raffaella Brugnoni, Giulia Ricci, Gabriele Siciliano

Research output: Contribution to journalArticlepeer-review

Abstract

Mutations of the main voltage-gated K channel members Kv1.1 are linked to several clinical conditions, such as periodic ataxia type 1, myokymia and seizure disorders. Due to their role in active magnesium reabsorption through the renal distal convoluted tubule segment, mutations in the KCNA1 gene encoding for Kv1.1 has been associated with hypomagnesemia with myokymia and tetanic crises. Here we describe a case of a young female patient who came to our attention for a history of muscular spasms, tetanic episodes and muscle weakness, initially misdiagnosed for fibromyalgia. After a genetic screening she was found to be carrier of the c.736A > G (p.Asn255Asp) mutation in KCNA1, previously described in a family with autosomal dominant hypomagnesemia with muscular spasms, myokymia and tetanic episodes. However, our patient has always presented normal serum and urinary magnesium values, whereas she was affected by hypocalcemia. Calcium supplementation gave only partial clinical benefit, with an improvement on tetanic episodes yet without a clinical remission of her spasms, whereas magnesium supplementation worsened her muscular symptomatology.

Original languageEnglish
Pages (from-to)36-39
Number of pages4
JournalActa Myologica
Volume39
Issue number1
DOIs
Publication statusPublished - 2020

Keywords

  • Hypomagnesemia
  • KCNA1
  • Tetany

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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