Affiliations 

  • 1 Department of Obstetrics and Gynaecology, Sibu Hospital, Sibu, Sarawak, Malaysia
  • 2 Faculty of Medicine, SEGi University Sibu Clinical Campus, Sibu, Sarawak, Malaysia
  • 3 Department of Obstetrics and Gynaecology, Sarikei Hospital, Sarikei, Sarawak, Malaysia
BMJ Case Rep, 2018 Jun 04;2018.
PMID: 29866669 DOI: 10.1136/bcr-2017-223588

Abstract

Hyperkalaemic periodic paralysis is a rare skeletal muscle disorder which is characterised by episodic muscle paralysis associated with hyperkalaemia. Although it is an autosomal-dominant disease, cases of de novo mutations have been reported. We report the case of a 30-year-old woman, gravida 5 para 3+1, who was planned for an elective repeated caesarean section at 38 weeks and 3 days of pregnancy. She developed recurrent episodes of hyperkalaemic periodic paralysis after receiving corticosteroids. Intravenous calcium gluconate was administered to normalise potassium levels (from 6.3 mmol/L to 4.1 mmol/L). Extra anaesthetic precautions were taken during the caesarean delivery. Postoperatively, she was well and discharged from the ward. She encountered similar symptoms in her third pregnancy, and there was no family history of muscle weakness which suggested a de novo mutation. Pregnancy seemed to result in vulnerability to hyperkalaemic attacks as she was never symptomatic outside pregnancy.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.