Satoyoshi Syndrome: Difficult to find or treat?
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.
Authors
- Niladri Sekhar Bhunia (ORCID: https://orcid.org/0000-0003-4126-3707)
- Rohit Bhowmick (ORCID: https://orcid.org/0000-0002-2589-4499)
- Aditi Das (ORCID: https://orcid.org/0000-0002-6731-6726)
- Avisek Majumder (ORCID: https://orcid.org/0000-0002-6761-2242)
- Subhankar Sarkar (ORCID: https://orcid.org/0000-0002-1316-0666)
- Rimjhim Sonowal (ORCID: https://orcid.org/0000-0002-3115-4876)
Publication Details
- Journal
- Indian Journal of Child Health
- Published
- 2025-09-26
- DOI
- https://doi.org/10.32677/ijch.v12i9.7720
- Primary Topic
- Myasthenia Gravis and Thymoma
- Type
- article
- Field-Weighted Citation Impact
- 0.00