Ross syndrome: a case report

Authors

  • Manoj Kr. Mahata Department of Neurosurgery, Hyogo College of Medicine, Hyogo, Japan
  • Saikat Ghosh Department of Neurology, Manorama Hospitex, Nadia, West Bengal, India
  • K. C. Ghosh Department of Neurology, CNMC, Kolkata, West Bengal, India
  • R. Bhattacharyya Department of Neurology, CNMC, Kolkata, West Bengal, India
  • G. P. Mondal Department of Neurology, CNMC, Kolkata, West Bengal, India

DOI:

https://doi.org/10.18203/2320-6012.ijrms20192928

Keywords:

Anhidrosis, Areflexia, Ross syndrome

Abstract

Ross syndrome is a rare partial dysautonomic syndrome of unknown aetiology, characterized by segmental hypo/ anhidrosis associated with Holmes-Adie syndrome (tonic pupil and hypo/areflexia). The hypohydrosis or anhydrosis is patchy initially, later it becomes segmental or diffuse. This is due to affection of postganglionic cholinergic parasympathetic and sympathetic fibers involvement. There are a very few cases (approximately 50) have been reported in the literature since its original description. Author report a 22 years old male with classical features of Ross syndrome.

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References

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Published

2019-06-28

How to Cite

Mahata, M. K., Ghosh, S., Ghosh, K. C., Bhattacharyya, R., & Mondal, G. P. (2019). Ross syndrome: a case report. International Journal of Research in Medical Sciences, 7(7), 2833–2834. https://doi.org/10.18203/2320-6012.ijrms20192928

Issue

Section

Case Reports