Isolated Sulfite Oxidase Deficiency: MR Imaging Features
Isolated sulfite oxidase deficiency is a rare autosomal inherited disorder of the normal degradation of sulfur-containing amino acids. Premature death in infancy secondary to severe neurologic deterioration is the usual outcome. This article provides an analysis, in temporal form, of brain imaging f...
Gespeichert in:
Veröffentlicht in: | American journal of neuroradiology : AJNR 2002-03, Vol.23 (3), p.484-485 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 485 |
---|---|
container_issue | 3 |
container_start_page | 484 |
container_title | American journal of neuroradiology : AJNR |
container_volume | 23 |
creator | Dublin, Arthur B Hald, John K Wootton-Gorges, Sandra L |
description | Isolated sulfite oxidase deficiency is a rare autosomal inherited disorder of the normal degradation of sulfur-containing amino acids. Premature death in infancy secondary to severe neurologic deterioration is the usual outcome. This article provides an analysis, in temporal form, of brain imaging findings in this disorder. |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7975306</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71527902</sourcerecordid><originalsourceid>FETCH-LOGICAL-h322t-4cd1a195864b6c58df5dc48833b68987aa1b2d63f68f8eea9cb7cdd92ea4e4723</originalsourceid><addsrcrecordid>eNpVkMlKxEAQQIMozrj8guSit0AvSS8eBFFHBxTBBbw1le7KTEsn0XTiOH_viON2qkM93itqIxlTzUWmC_20mYwJ1UUmKFGjZCfGZ0JIoSXbTkaUakIJy8eJmsY2QI8uvR9C5XtMb9-9g4jpOVbeemzs8ji9uUunNcx8M0snCP3QYdxLtioIEffXczd5nFw8nF1l17eX07PT62zOGeuz3DoKqzOUyEthC-WqwtlcKc5LobSSALRkTvBKqEohgraltM5phpBjLhnfTU6-vC9DWaOz2PQdBPPS-Rq6pWnBm_-bxs_NrH0zUsuCE7ESHK0FXfs6YOxN7aPFEKDBdohG0oJJTT5LB39LP4nvZ62AwzUA0UKoOmisj78cL6SgnP9ycz-bL3yHJtYQwkpLzWKxYNxwk6ucfwAjj4Ft</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71527902</pqid></control><display><type>article</type><title>Isolated Sulfite Oxidase Deficiency: MR Imaging Features</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Dublin, Arthur B ; Hald, John K ; Wootton-Gorges, Sandra L</creator><creatorcontrib>Dublin, Arthur B ; Hald, John K ; Wootton-Gorges, Sandra L</creatorcontrib><description>Isolated sulfite oxidase deficiency is a rare autosomal inherited disorder of the normal degradation of sulfur-containing amino acids. Premature death in infancy secondary to severe neurologic deterioration is the usual outcome. This article provides an analysis, in temporal form, of brain imaging findings in this disorder.</description><identifier>ISSN: 0195-6108</identifier><identifier>EISSN: 1936-959X</identifier><identifier>PMID: 11901024</identifier><identifier>CODEN: AAJNDL</identifier><language>eng</language><publisher>Oak Brook, IL: Am Soc Neuroradiology</publisher><subject>Amino Acid Metabolism, Inborn Errors - diagnosis ; Aminoacid disorders ; Biological and medical sciences ; Brain - pathology ; Disease Progression ; Errors of metabolism ; Female ; Humans ; Infant, Newborn ; Magnetic Resonance Imaging ; Medical sciences ; Metabolic diseases ; Oxidoreductases Acting on Sulfur Group Donors - deficiency ; Pediatrics ; Seizures - etiology</subject><ispartof>American journal of neuroradiology : AJNR, 2002-03, Vol.23 (3), p.484-485</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright © American Society of Neuroradiology 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7975306/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7975306/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13576133$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11901024$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dublin, Arthur B</creatorcontrib><creatorcontrib>Hald, John K</creatorcontrib><creatorcontrib>Wootton-Gorges, Sandra L</creatorcontrib><title>Isolated Sulfite Oxidase Deficiency: MR Imaging Features</title><title>American journal of neuroradiology : AJNR</title><addtitle>AJNR Am J Neuroradiol</addtitle><description>Isolated sulfite oxidase deficiency is a rare autosomal inherited disorder of the normal degradation of sulfur-containing amino acids. Premature death in infancy secondary to severe neurologic deterioration is the usual outcome. This article provides an analysis, in temporal form, of brain imaging findings in this disorder.</description><subject>Amino Acid Metabolism, Inborn Errors - diagnosis</subject><subject>Aminoacid disorders</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Disease Progression</subject><subject>Errors of metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Magnetic Resonance Imaging</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Oxidoreductases Acting on Sulfur Group Donors - deficiency</subject><subject>Pediatrics</subject><subject>Seizures - etiology</subject><issn>0195-6108</issn><issn>1936-959X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMlKxEAQQIMozrj8guSit0AvSS8eBFFHBxTBBbw1le7KTEsn0XTiOH_viON2qkM93itqIxlTzUWmC_20mYwJ1UUmKFGjZCfGZ0JIoSXbTkaUakIJy8eJmsY2QI8uvR9C5XtMb9-9g4jpOVbeemzs8ji9uUunNcx8M0snCP3QYdxLtioIEffXczd5nFw8nF1l17eX07PT62zOGeuz3DoKqzOUyEthC-WqwtlcKc5LobSSALRkTvBKqEohgraltM5phpBjLhnfTU6-vC9DWaOz2PQdBPPS-Rq6pWnBm_-bxs_NrH0zUsuCE7ESHK0FXfs6YOxN7aPFEKDBdohG0oJJTT5LB39LP4nvZ62AwzUA0UKoOmisj78cL6SgnP9ycz-bL3yHJtYQwkpLzWKxYNxwk6ucfwAjj4Ft</recordid><startdate>20020301</startdate><enddate>20020301</enddate><creator>Dublin, Arthur B</creator><creator>Hald, John K</creator><creator>Wootton-Gorges, Sandra L</creator><general>Am Soc Neuroradiology</general><general>American Society of Neuroradiology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20020301</creationdate><title>Isolated Sulfite Oxidase Deficiency: MR Imaging Features</title><author>Dublin, Arthur B ; Hald, John K ; Wootton-Gorges, Sandra L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h322t-4cd1a195864b6c58df5dc48833b68987aa1b2d63f68f8eea9cb7cdd92ea4e4723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino Acid Metabolism, Inborn Errors - diagnosis</topic><topic>Aminoacid disorders</topic><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Disease Progression</topic><topic>Errors of metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Magnetic Resonance Imaging</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Oxidoreductases Acting on Sulfur Group Donors - deficiency</topic><topic>Pediatrics</topic><topic>Seizures - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dublin, Arthur B</creatorcontrib><creatorcontrib>Hald, John K</creatorcontrib><creatorcontrib>Wootton-Gorges, Sandra L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of neuroradiology : AJNR</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dublin, Arthur B</au><au>Hald, John K</au><au>Wootton-Gorges, Sandra L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolated Sulfite Oxidase Deficiency: MR Imaging Features</atitle><jtitle>American journal of neuroradiology : AJNR</jtitle><addtitle>AJNR Am J Neuroradiol</addtitle><date>2002-03-01</date><risdate>2002</risdate><volume>23</volume><issue>3</issue><spage>484</spage><epage>485</epage><pages>484-485</pages><issn>0195-6108</issn><eissn>1936-959X</eissn><coden>AAJNDL</coden><abstract>Isolated sulfite oxidase deficiency is a rare autosomal inherited disorder of the normal degradation of sulfur-containing amino acids. Premature death in infancy secondary to severe neurologic deterioration is the usual outcome. This article provides an analysis, in temporal form, of brain imaging findings in this disorder.</abstract><cop>Oak Brook, IL</cop><pub>Am Soc Neuroradiology</pub><pmid>11901024</pmid><tpages>2</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0195-6108 |
ispartof | American journal of neuroradiology : AJNR, 2002-03, Vol.23 (3), p.484-485 |
issn | 0195-6108 1936-959X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7975306 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Amino Acid Metabolism, Inborn Errors - diagnosis Aminoacid disorders Biological and medical sciences Brain - pathology Disease Progression Errors of metabolism Female Humans Infant, Newborn Magnetic Resonance Imaging Medical sciences Metabolic diseases Oxidoreductases Acting on Sulfur Group Donors - deficiency Pediatrics Seizures - etiology |
title | Isolated Sulfite Oxidase Deficiency: MR Imaging Features |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-18T21%3A54%3A46IST&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=Isolated%20Sulfite%20Oxidase%20Deficiency:%20MR%20Imaging%20Features&rft.jtitle=American%20journal%20of%20neuroradiology%20:%20AJNR&rft.au=Dublin,%20Arthur%20B&rft.date=2002-03-01&rft.volume=23&rft.issue=3&rft.spage=484&rft.epage=485&rft.pages=484-485&rft.issn=0195-6108&rft.eissn=1936-959X&rft.coden=AAJNDL&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E71527902%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=71527902&rft_id=info:pmid/11901024&rfr_iscdi=true |