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Treatment of Satoyoshi syndrome: a systematic review.
Solís-García Del Pozo J, de Cabo C, Solera J. Solís-García Del Pozo J, et al. Orphanet J Rare Dis. 2019 Jun 19;14(1):146. doi: 10.1186/s13023-019-1120-7. Orphanet J Rare Dis. 2019. PMID: 31217029 Free PMC article. Review.
BACKGROUND: Satoyoshi syndrome is a multisystemic rare disease of unknown etiology, although an autoimmune basis is presumed. ...A review of treatment and its response is still pending. RESULTS: Sixty-four cases of Satoyoshi syndrome were published bet …
BACKGROUND: Satoyoshi syndrome is a multisystemic rare disease of unknown etiology, although an autoimmune basis is presumed. …
Satoyoshi syndrome.
Mukhopadhyay D, Ghosh A, Mukhopadhyay M. Mukhopadhyay D, et al. Indian Pediatr. 2011 Sep;48(9):729-31. Indian Pediatr. 2011. PMID: 21992906
Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. ...
Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skele …
Is Satoyoshi syndrome an autoimmune disease? A systematic review.
Viana Abreu Montanaro V, Solís-García Del Pozo J, Falcão Hora T, León BH, de Cabo C, Solera J. Viana Abreu Montanaro V, et al. Rheumatology (Oxford). 2023 Jul 5;62(7):2343-2351. doi: 10.1093/rheumatology/kead067. Rheumatology (Oxford). 2023. PMID: 36749015
OBJECTIVES: Satoyoshi syndrome is a rare multisystem disease of presumed autoimmune aetiology. We carried out a systematic review to evaluate the available evidence to support that autoimmune hypothesis. METHODS: We searched for Satoyoshi syndrome case …
OBJECTIVES: Satoyoshi syndrome is a rare multisystem disease of presumed autoimmune aetiology. We carried out a systematic rev …
Satoyoshi syndrome.
Ashalatha R, Kishore A, Sarada C, Nair MD. Ashalatha R, et al. Neurol India. 2004 Mar;52(1):94-5. Neurol India. 2004. PMID: 15069249 Free article.
Satoyoshi syndrome (Komuragaeri disease) is a rare disorder of presumed autoimmune etiology, characterized by painful muscle spasms, alopecia, diarrhea, endocrinopathy with amenorrhoea and secondary skeletal abnormalities. ...
Satoyoshi syndrome (Komuragaeri disease) is a rare disorder of presumed autoimmune etiology, characterized by painful muscle s …
Satoyoshi syndrome-A case report from India.
Mani V, George R. Mani V, et al. Pediatr Dermatol. 2017 Nov;34(6):e296-e298. doi: 10.1111/pde.13271. Epub 2017 Sep 22. Pediatr Dermatol. 2017. PMID: 28940615
We report an 11-year-old girl with Satoyoshi syndrome who presented to the dermatology department for treatment of alopecia universalis. We present this case to emphasize the importance of recognizing Satoyoshi syndrome, which could go unnoticed if not …
We report an 11-year-old girl with Satoyoshi syndrome who presented to the dermatology department for treatment of alopecia un …
Intravenous gammaglobulin therapy of Satoyoshi syndrome.
Arita J, Hamano S, Nara T, Maekawa K. Arita J, et al. Brain Dev. 1996 Sep-Oct;18(5):409-11. doi: 10.1016/0387-7604(96)00033-2. Brain Dev. 1996. PMID: 8891238
Satoyoshi syndrome is a very rare disease of unknown etiology, characterized by intermittent painful muscle spasms, alopecia, multiple epiphyseal changes, diarrhea and endocrine disorders. ...This is the first report of gammaglobulin therapy of Satoyoshi s …
Satoyoshi syndrome is a very rare disease of unknown etiology, characterized by intermittent painful muscle spasms, alopecia, …
Satoyoshi syndrome: a rare multisystemic disorder requiring systemic and symptomatic treatment.
Heger S, Kuester RM, Volk R, Stephani U, Sippell WG. Heger S, et al. Brain Dev. 2006 Jun;28(5):300-4. doi: 10.1016/j.braindev.2005.10.006. Epub 2006 Feb 14. Brain Dev. 2006. PMID: 16478652
Satoyoshi syndrome is a rare multisystemic disorder with assumed autoimmune pathogenesis. Typical clinical features are progressive painful muscle spasms, alopecia, diarrhoea, and skeletal and endocrine abnormalities often resulting in early invalidism and de …
Satoyoshi syndrome is a rare multisystemic disorder with assumed autoimmune pathogenesis. Typical clinical features are …
Satoyoshi Syndrome with Progressive Orofacial Manifestations: A Case History Report.
Li J, Peng D, Jiang T, Avivi-Arber L. Li J, et al. Int J Prosthodont. 2017 Mar/Apr;30(2):163-167. doi: 10.11607/ijp.4905. Int J Prosthodont. 2017. PMID: 28267828
A young female patient suffering from Satoyoshi syndrome had the first characteristic signs and symptoms of hair loss and progressive spontaneous intermittent painful spasms of limb muscles at age 6.5 years. ...
A young female patient suffering from Satoyoshi syndrome had the first characteristic signs and symptoms of hair loss and prog …
Radiological and orthopedic abnormalities in Satoyoshi syndrome.
Haymon M, Willis RB, Ehlayel MS, Lacassie Y. Haymon M, et al. Pediatr Radiol. 1997 May;27(5):415-8. doi: 10.1007/s002470050158. Pediatr Radiol. 1997. PMID: 9133353
Satoyoshi syndrome is a rare disorder of unknown etiology characterized by progressive, painful intermittent muscle spasms, severe skeletal abnormalities mimicking a skeletal dysplasia, malabsorption, alopecia, and amenorrhea. ...
Satoyoshi syndrome is a rare disorder of unknown etiology characterized by progressive, painful intermittent muscle spasms, se …
A case of Satoyoshi syndrome: a multisystem disorder.
Kamat D, Petry L, Berry S. Kamat D, et al. Clin Pediatr (Phila). 2003 Oct;42(8):745-8. doi: 10.1177/000992280304200811. Clin Pediatr (Phila). 2003. PMID: 14601924
A 14-year-old boy with Satoyoshi syndrome is reported. Less than 50 patients with Satoyoshi syndrome have been reported in the world literature. This patient had alopecia, muscle spasms, and skeletal abnormalities, which are three of the most common …
A 14-year-old boy with Satoyoshi syndrome is reported. Less than 50 patients with Satoyoshi syndrome have been r …
13 results