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Satoyoshi syndrome-A case report from India.
Pediatr Dermatol. 2017 Nov; 34(6):e296-e298.PD

Abstract

Satoyoshi syndrome was first reported in Japan in 1967. It is a rare multisystem disorder of presumed autoimmune etiology that is characterized by alopecia, intermittent painful muscle spasms, diarrhea, and antinuclear antibody positivity. 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 suspected.

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Authors+Show Affiliations

Mani V
Department of Dermatology, Venereology & Leprosy, Christian Medical College and Hospital, Vellore, TN, India.
George R
Department of Dermatology, Venereology & Leprosy, Christian Medical College and Hospital, Vellore, TN, India.

MeSH

AlopeciaBone and BonesChildDiarrheaFemaleGlucocorticoidsHumansIndiaSpasm

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

28940615

Citation

Mani, Venkatraman, and Renu George. "Satoyoshi syndrome-A Case Report From India." Pediatric Dermatology, vol. 34, no. 6, 2017, pp. e296-e298.
Mani V, George R. Satoyoshi syndrome-A case report from India. Pediatr Dermatol. 2017;34(6):e296-e298.
Mani, V., & George, R. (2017). Satoyoshi syndrome-A case report from India. Pediatric Dermatology, 34(6), e296-e298. https://doi.org/10.1111/pde.13271
Mani V, George R. Satoyoshi syndrome-A Case Report From India. Pediatr Dermatol. 2017;34(6):e296-e298. PubMed PMID: 28940615.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Satoyoshi syndrome-A case report from India. AU - Mani,Venkatraman, AU - George,Renu, Y1 - 2017/09/22/ PY - 2017/9/25/pubmed PY - 2018/6/13/medline PY - 2017/9/24/entrez KW - Satoyoshi syndrome KW - alopecia universalis KW - multisystem involvement SP - e296 EP - e298 JF - Pediatric dermatology JO - Pediatr Dermatol VL - 34 IS - 6 N2 - Satoyoshi syndrome was first reported in Japan in 1967. It is a rare multisystem disorder of presumed autoimmune etiology that is characterized by alopecia, intermittent painful muscle spasms, diarrhea, and antinuclear antibody positivity. 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 suspected. SN - 1525-1470 UR - https://www.unboundmedicine.com/medline/citation/28940615/Satoyoshi_syndrome-A_case_report_from_India L2 - https://doi.org/10.1111/pde.13271 DB - PRIME DP - Unbound Medicine ER -