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Ross Syndrome: A Patient with a 23-Year History

  • Zuhal Filikci*
  • , Hans-Henrik Horsten
  • , Mette Lindelof
  • *Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

Abstract

We present a 60-year-old female with a 23-year history of anhidrosis with concomitant heat intolerance. At examination, we found a right-sided tonic pupil, absent tendon reflexes, and a segmental patch of compensatory hyperhidrosis in the left lower quadrant of her trunk. To further confirm this finding, a minor test (a starch-iodine test, which is used to evaluate the sudomotor function, sweating) was performed. Nerve conduction studies revealed evidence of a mild distal sensory polyneuropathy of the axonal type. Tilt-table testing showed signs of orthostatic hypotension with evidence of reduced sympathetic function. Skin biopsy excluded pathology in the sweat glands. Our patient met the criteria for a diagnosis of Ross syndrome. This case describes the long-term outcome of this rare entity and highlights how careful examination and bedside autonomic testing can confirm the diagnosis of autonomic neurological disorders.

Original languageEnglish
Pages (from-to)132-135
Number of pages4
JournalCase Reports in Neurology
Volume12
Issue number1
DOIs
Publication statusPublished - 2020

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