A case of Gitelman syndrome associated with idiopathic intracranial hypertension

Intern Med. 2011;50(14):1493-6. doi: 10.2169/internalmedicine.50.5305. Epub 2011 Jul 15.

Abstract

An 18-year-old woman with Gitelman syndrome (GS) associated with idiopathic intracranial hypertension (IIH) is described. She was obese and showed a 10 kg gain in body weight over a period of 8 months. She presented with headache, vomiting, and diplopia. She had bilateral papilledema, and right abducens palsy. CSF examination demonstrated high pressure (over 320 mmH(2)O) with normal cytochemistry. Brain MRI was normal. She showed mild alkalosis, hypokalemia, hypomagnesemia, increased plasma renin activity, and normal blood pressure. Two heterozygous mutations in the SLC12A3 gene were identified. Therefore, she was diagnosed as GS with IIH. We should keep in mind the possible occurrence of IIH in GS.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Amino Acid Substitution
  • Base Sequence
  • DNA Mutational Analysis
  • Exons
  • Female
  • Gitelman Syndrome / complications*
  • Gitelman Syndrome / diagnosis
  • Gitelman Syndrome / genetics
  • Heterozygote
  • Humans
  • Mutation, Missense
  • Pseudotumor Cerebri / complications*
  • Pseudotumor Cerebri / diagnosis
  • Pseudotumor Cerebri / genetics
  • Receptors, Drug / genetics
  • Solute Carrier Family 12, Member 3
  • Symporters / genetics

Substances

  • Receptors, Drug
  • SLC12A3 protein, human
  • Solute Carrier Family 12, Member 3
  • Symporters