Loading…
Satoyoshi syndrome
Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. We report a 11 year old girl presenting with the typical features of alopecia totalis, severe muscle spasm and skeletal deformities.
Saved in:
Published in: | Indian pediatrics 2011-09, Vol.48 (9), p.729-731 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 731 |
container_issue | 9 |
container_start_page | 729 |
container_title | Indian pediatrics |
container_volume | 48 |
creator | Mukhopadhyay, Debadatta Ghosh, Apurba Mukhopadhyay, Maya |
description | Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. We report a 11 year old girl presenting with the typical features of alopecia totalis, severe muscle spasm and skeletal deformities. |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_898500915</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>898500915</sourcerecordid><originalsourceid>FETCH-LOGICAL-p210t-9dcc4741b2b15a26e4608963dbe957b438cf38b3e4f3e28678c2d588738136833</originalsourceid><addsrcrecordid>eNo1j8tKw0AUQAdB2tq68QPEnavAzNx53FlK8VEouFDXYR43GEk6MZMs8vcK1tXZHA6cC7bhzqrKau3W7KqUL84lSC1WbC2Fc9Jxs2E3b37KSy6f7V1ZTmnMPe3YZeO7QtdnbtnH0-P7_qU6vj4f9g_HapCCT5VLMSqrRJBBaC8NKcPRGUiBnLZBAcYGMACpBkiisRhl0ogWUIBBgC27_-sOY_6eqUx135ZIXedPlOdSo0PNuRP617w9m3PoKdXD2PZ-XOr_DfgB1llAFQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>898500915</pqid></control><display><type>article</type><title>Satoyoshi syndrome</title><source>Springer Link</source><source>Alma/SFX Local Collection</source><creator>Mukhopadhyay, Debadatta ; Ghosh, Apurba ; Mukhopadhyay, Maya</creator><creatorcontrib>Mukhopadhyay, Debadatta ; Ghosh, Apurba ; Mukhopadhyay, Maya</creatorcontrib><description>Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. We report a 11 year old girl presenting with the typical features of alopecia totalis, severe muscle spasm and skeletal deformities.</description><identifier>EISSN: 0974-7559</identifier><identifier>PMID: 21992906</identifier><language>eng</language><publisher>India</publisher><subject>Alopecia - diagnosis ; Alopecia - drug therapy ; Alopecia - pathology ; Alopecia - physiopathology ; Bone and Bones - abnormalities ; Bone and Bones - pathology ; Bone and Bones - physiopathology ; Child ; Diarrhea - diagnosis ; Diarrhea - drug therapy ; Diarrhea - pathology ; Diarrhea - physiopathology ; Female ; Humans ; Phenytoin - therapeutic use ; Prednisolone - therapeutic use ; Spasm - diagnosis ; Spasm - drug therapy ; Spasm - pathology ; Spasm - physiopathology ; Vitamin D - therapeutic use</subject><ispartof>Indian pediatrics, 2011-09, Vol.48 (9), p.729-731</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21992906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukhopadhyay, Debadatta</creatorcontrib><creatorcontrib>Ghosh, Apurba</creatorcontrib><creatorcontrib>Mukhopadhyay, Maya</creatorcontrib><title>Satoyoshi syndrome</title><title>Indian pediatrics</title><addtitle>Indian Pediatr</addtitle><description>Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. We report a 11 year old girl presenting with the typical features of alopecia totalis, severe muscle spasm and skeletal deformities.</description><subject>Alopecia - diagnosis</subject><subject>Alopecia - drug therapy</subject><subject>Alopecia - pathology</subject><subject>Alopecia - physiopathology</subject><subject>Bone and Bones - abnormalities</subject><subject>Bone and Bones - pathology</subject><subject>Bone and Bones - physiopathology</subject><subject>Child</subject><subject>Diarrhea - diagnosis</subject><subject>Diarrhea - drug therapy</subject><subject>Diarrhea - pathology</subject><subject>Diarrhea - physiopathology</subject><subject>Female</subject><subject>Humans</subject><subject>Phenytoin - therapeutic use</subject><subject>Prednisolone - therapeutic use</subject><subject>Spasm - diagnosis</subject><subject>Spasm - drug therapy</subject><subject>Spasm - pathology</subject><subject>Spasm - physiopathology</subject><subject>Vitamin D - therapeutic use</subject><issn>0974-7559</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNo1j8tKw0AUQAdB2tq68QPEnavAzNx53FlK8VEouFDXYR43GEk6MZMs8vcK1tXZHA6cC7bhzqrKau3W7KqUL84lSC1WbC2Fc9Jxs2E3b37KSy6f7V1ZTmnMPe3YZeO7QtdnbtnH0-P7_qU6vj4f9g_HapCCT5VLMSqrRJBBaC8NKcPRGUiBnLZBAcYGMACpBkiisRhl0ogWUIBBgC27_-sOY_6eqUx135ZIXedPlOdSo0PNuRP617w9m3PoKdXD2PZ-XOr_DfgB1llAFQ</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Mukhopadhyay, Debadatta</creator><creator>Ghosh, Apurba</creator><creator>Mukhopadhyay, Maya</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20110901</creationdate><title>Satoyoshi syndrome</title><author>Mukhopadhyay, Debadatta ; Ghosh, Apurba ; Mukhopadhyay, Maya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p210t-9dcc4741b2b15a26e4608963dbe957b438cf38b3e4f3e28678c2d588738136833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Alopecia - diagnosis</topic><topic>Alopecia - drug therapy</topic><topic>Alopecia - pathology</topic><topic>Alopecia - physiopathology</topic><topic>Bone and Bones - abnormalities</topic><topic>Bone and Bones - pathology</topic><topic>Bone and Bones - physiopathology</topic><topic>Child</topic><topic>Diarrhea - diagnosis</topic><topic>Diarrhea - drug therapy</topic><topic>Diarrhea - pathology</topic><topic>Diarrhea - physiopathology</topic><topic>Female</topic><topic>Humans</topic><topic>Phenytoin - therapeutic use</topic><topic>Prednisolone - therapeutic use</topic><topic>Spasm - diagnosis</topic><topic>Spasm - drug therapy</topic><topic>Spasm - pathology</topic><topic>Spasm - physiopathology</topic><topic>Vitamin D - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukhopadhyay, Debadatta</creatorcontrib><creatorcontrib>Ghosh, Apurba</creatorcontrib><creatorcontrib>Mukhopadhyay, Maya</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Indian pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukhopadhyay, Debadatta</au><au>Ghosh, Apurba</au><au>Mukhopadhyay, Maya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Satoyoshi syndrome</atitle><jtitle>Indian pediatrics</jtitle><addtitle>Indian Pediatr</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>48</volume><issue>9</issue><spage>729</spage><epage>731</epage><pages>729-731</pages><eissn>0974-7559</eissn><abstract>Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. We report a 11 year old girl presenting with the typical features of alopecia totalis, severe muscle spasm and skeletal deformities.</abstract><cop>India</cop><pmid>21992906</pmid><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | EISSN: 0974-7559 |
ispartof | Indian pediatrics, 2011-09, Vol.48 (9), p.729-731 |
issn | 0974-7559 |
language | eng |
recordid | cdi_proquest_miscellaneous_898500915 |
source | Springer Link; Alma/SFX Local Collection |
subjects | Alopecia - diagnosis Alopecia - drug therapy Alopecia - pathology Alopecia - physiopathology Bone and Bones - abnormalities Bone and Bones - pathology Bone and Bones - physiopathology Child Diarrhea - diagnosis Diarrhea - drug therapy Diarrhea - pathology Diarrhea - physiopathology Female Humans Phenytoin - therapeutic use Prednisolone - therapeutic use Spasm - diagnosis Spasm - drug therapy Spasm - pathology Spasm - physiopathology Vitamin D - therapeutic use |
title | Satoyoshi syndrome |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T02%3A08%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Satoyoshi%20syndrome&rft.jtitle=Indian%20pediatrics&rft.au=Mukhopadhyay,%20Debadatta&rft.date=2011-09-01&rft.volume=48&rft.issue=9&rft.spage=729&rft.epage=731&rft.pages=729-731&rft.eissn=0974-7559&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E898500915%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p210t-9dcc4741b2b15a26e4608963dbe957b438cf38b3e4f3e28678c2d588738136833%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=898500915&rft_id=info:pmid/21992906&rfr_iscdi=true |