Satoyoshi Syndrome: Difficult to find or treat?

Authors

  • Ashik Majumder
  • Aditi Das
  • Rohit Bhowmick
  • Niladri Sekhar Bhunia
  • Subhankar Sarkar
  • Rimjhim Sonowal

DOI:

https://doi.org/10.32677/ijch.v12i9.7720

Keywords:

Satoyoshi syndrome, a multisystemic, autoimmune disorder, autoantibodies, alopecia, and muscle spasm

Abstract

Satoyoshi Syndrome, also known as Komuragaeri disease, is a rare multisystemic autoimmune disorder characterised by alopecia, intermittent painful muscle spasms, diarrhoea, endocrinopathies, skeletal deformities, and positivity for antinuclear antibodies (ANA). The etiology of this condition remains unclear. This case report discusses Satoyoshi Syndrome in a 10-year-old girl, emphasising the diagnostic challenge, clinical course, treatments, and outcomes.

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Published

2025-09-26

Issue

Vol. 12 No. 9 (2025): September

Section

Case Reports

License

Copyright (c) 2025 Ashik Majumder, Aditi Das, Rohit Bhowmick, Niladri Sekhar Bhunia, Subhankar Sarkar, Rimjhim Sonowal

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

How to Cite

Majumder, A., Das, A., Bhowmick, R. ., Bhunia, N. S., Sarkar, S., & Sonowal, R. (2025). Satoyoshi Syndrome: Difficult to find or treat?. Indian Journal of Child Health, 12(9), 115-117. https://doi.org/10.32677/ijch.v12i9.7720