Transient trimethylaminuria in childhood

Trimethylaminuria, also called fish‐odour syndrome, is an inherited disorder caused by deficient N‐oxidation and increased excretion of trimethylamine. This study reports on two unrelated and otherwise healthy children with transient trimethylaminuria, a hitherto unknown abnormality, without N‐oxida...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Acta Paediatrica 1998-11, Vol.87 (11), p.1205-1207
Hauptverfasser: Mayatepek, E, Kohlmüller, D
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1207
container_issue 11
container_start_page 1205
container_title Acta Paediatrica
container_volume 87
creator Mayatepek, E
Kohlmüller, D
description Trimethylaminuria, also called fish‐odour syndrome, is an inherited disorder caused by deficient N‐oxidation and increased excretion of trimethylamine. This study reports on two unrelated and otherwise healthy children with transient trimethylaminuria, a hitherto unknown abnormality, without N‐oxidation deficiency. This demonstrates that a diagnosis offish‐odour syndrome should include the analysis of urinary excretion not only of trimethylamine but also of trimethylamine‐N‐oxide. Since transient trimethylaminuria may be a common condition and no cause for it can presently be recognized, such patients will require careful follow‐up.
doi_str_mv 10.1111/j.1651-2227.1998.tb00934.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70118479</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70118479</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5035-e34174bd87ddc19cde65c4b81f148499cc19ea7c994f2bd71b8e6cf7a79797863</originalsourceid><addsrcrecordid>eNqVkFFLwzAUhYMoc05_gjBExJfWpEmaxBcZQ6cwdJOJjyFNU5bZtbNpcfv3pqzMZ3MfAjnnnpv7AXCFYIj8uVuFKKYoiKKIhUgIHtYJhAKTcHsE-gfpGPQhhzigEcWn4My5FYQRFiTugZ7gJBYR74PbRaUKZ01RD-vKrk293OVqbYumsmpoi6Fe2jxdlmV6Dk4ylTtz0d0D8PH0uBg_B9O3yct4NA00hZgGBhPESJJylqYaCZ2amGqScJQhwokQ2j8axbQQJIuSlKGEm1hnTDHhi8d4AG72uZuq_G6Mq-XaOm3yXBWmbJxkECFOmPDG-71RV6Vzlcnkxi-gqp1EULaY5Eq2LGTLQraYZIdJbn3zZTelSdYmPbR2XLx-3enKaZVnHpK27m8C5QJB5m0Pe9uPzc3uHx-Qo9kIRZD6hGCfYF1ttocEVX3JmGFG5efrRM5nlDAC3-Uc_wKPwJMG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70118479</pqid></control><display><type>article</type><title>Transient trimethylaminuria in childhood</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Alma/SFX Local Collection</source><creator>Mayatepek, E ; Kohlmüller, D</creator><creatorcontrib>Mayatepek, E ; Kohlmüller, D</creatorcontrib><description>Trimethylaminuria, also called fish‐odour syndrome, is an inherited disorder caused by deficient N‐oxidation and increased excretion of trimethylamine. This study reports on two unrelated and otherwise healthy children with transient trimethylaminuria, a hitherto unknown abnormality, without N‐oxidation deficiency. This demonstrates that a diagnosis offish‐odour syndrome should include the analysis of urinary excretion not only of trimethylamine but also of trimethylamine‐N‐oxide. Since transient trimethylaminuria may be a common condition and no cause for it can presently be recognized, such patients will require careful follow‐up.</description><identifier>ISSN: 0803-5253</identifier><identifier>EISSN: 1651-2227</identifier><identifier>DOI: 10.1111/j.1651-2227.1998.tb00934.x</identifier><identifier>PMID: 9846928</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Medical sciences ; Metabolic diseases ; Metabolism, Inborn Errors - urine ; Methylamines - urine ; Miscellaneous ; Odorants ; Other metabolic disorders ; Time Factors ; Trimethylamine ; trimethylamine-N-oxide ; trimethylaminuria</subject><ispartof>Acta Paediatrica, 1998-11, Vol.87 (11), p.1205-1207</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5035-e34174bd87ddc19cde65c4b81f148499cc19ea7c994f2bd71b8e6cf7a79797863</citedby><cites>FETCH-LOGICAL-c5035-e34174bd87ddc19cde65c4b81f148499cc19ea7c994f2bd71b8e6cf7a79797863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1651-2227.1998.tb00934.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1651-2227.1998.tb00934.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1589107$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9846928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mayatepek, E</creatorcontrib><creatorcontrib>Kohlmüller, D</creatorcontrib><title>Transient trimethylaminuria in childhood</title><title>Acta Paediatrica</title><addtitle>Acta Paediatr</addtitle><description>Trimethylaminuria, also called fish‐odour syndrome, is an inherited disorder caused by deficient N‐oxidation and increased excretion of trimethylamine. This study reports on two unrelated and otherwise healthy children with transient trimethylaminuria, a hitherto unknown abnormality, without N‐oxidation deficiency. This demonstrates that a diagnosis offish‐odour syndrome should include the analysis of urinary excretion not only of trimethylamine but also of trimethylamine‐N‐oxide. Since transient trimethylaminuria may be a common condition and no cause for it can presently be recognized, such patients will require careful follow‐up.</description><subject>Biological and medical sciences</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Metabolism, Inborn Errors - urine</subject><subject>Methylamines - urine</subject><subject>Miscellaneous</subject><subject>Odorants</subject><subject>Other metabolic disorders</subject><subject>Time Factors</subject><subject>Trimethylamine</subject><subject>trimethylamine-N-oxide</subject><subject>trimethylaminuria</subject><issn>0803-5253</issn><issn>1651-2227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkFFLwzAUhYMoc05_gjBExJfWpEmaxBcZQ6cwdJOJjyFNU5bZtbNpcfv3pqzMZ3MfAjnnnpv7AXCFYIj8uVuFKKYoiKKIhUgIHtYJhAKTcHsE-gfpGPQhhzigEcWn4My5FYQRFiTugZ7gJBYR74PbRaUKZ01RD-vKrk293OVqbYumsmpoi6Fe2jxdlmV6Dk4ylTtz0d0D8PH0uBg_B9O3yct4NA00hZgGBhPESJJylqYaCZ2amGqScJQhwokQ2j8axbQQJIuSlKGEm1hnTDHhi8d4AG72uZuq_G6Mq-XaOm3yXBWmbJxkECFOmPDG-71RV6Vzlcnkxi-gqp1EULaY5Eq2LGTLQraYZIdJbn3zZTelSdYmPbR2XLx-3enKaZVnHpK27m8C5QJB5m0Pe9uPzc3uHx-Qo9kIRZD6hGCfYF1ttocEVX3JmGFG5efrRM5nlDAC3-Uc_wKPwJMG</recordid><startdate>199811</startdate><enddate>199811</enddate><creator>Mayatepek, E</creator><creator>Kohlmüller, D</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199811</creationdate><title>Transient trimethylaminuria in childhood</title><author>Mayatepek, E ; Kohlmüller, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5035-e34174bd87ddc19cde65c4b81f148499cc19ea7c994f2bd71b8e6cf7a79797863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Metabolism, Inborn Errors - urine</topic><topic>Methylamines - urine</topic><topic>Miscellaneous</topic><topic>Odorants</topic><topic>Other metabolic disorders</topic><topic>Time Factors</topic><topic>Trimethylamine</topic><topic>trimethylamine-N-oxide</topic><topic>trimethylaminuria</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mayatepek, E</creatorcontrib><creatorcontrib>Kohlmüller, D</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Acta Paediatrica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mayatepek, E</au><au>Kohlmüller, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transient trimethylaminuria in childhood</atitle><jtitle>Acta Paediatrica</jtitle><addtitle>Acta Paediatr</addtitle><date>1998-11</date><risdate>1998</risdate><volume>87</volume><issue>11</issue><spage>1205</spage><epage>1207</epage><pages>1205-1207</pages><issn>0803-5253</issn><eissn>1651-2227</eissn><abstract>Trimethylaminuria, also called fish‐odour syndrome, is an inherited disorder caused by deficient N‐oxidation and increased excretion of trimethylamine. This study reports on two unrelated and otherwise healthy children with transient trimethylaminuria, a hitherto unknown abnormality, without N‐oxidation deficiency. This demonstrates that a diagnosis offish‐odour syndrome should include the analysis of urinary excretion not only of trimethylamine but also of trimethylamine‐N‐oxide. Since transient trimethylaminuria may be a common condition and no cause for it can presently be recognized, such patients will require careful follow‐up.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9846928</pmid><doi>10.1111/j.1651-2227.1998.tb00934.x</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0803-5253
ispartof Acta Paediatrica, 1998-11, Vol.87 (11), p.1205-1207
issn 0803-5253
1651-2227
language eng
recordid cdi_proquest_miscellaneous_70118479
source MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects Biological and medical sciences
Child, Preschool
Female
Humans
Infant
Male
Medical sciences
Metabolic diseases
Metabolism, Inborn Errors - urine
Methylamines - urine
Miscellaneous
Odorants
Other metabolic disorders
Time Factors
Trimethylamine
trimethylamine-N-oxide
trimethylaminuria
title Transient trimethylaminuria in childhood
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T10%3A27%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Transient%20trimethylaminuria%20in%20childhood&rft.jtitle=Acta%20Paediatrica&rft.au=Mayatepek,%20E&rft.date=1998-11&rft.volume=87&rft.issue=11&rft.spage=1205&rft.epage=1207&rft.pages=1205-1207&rft.issn=0803-5253&rft.eissn=1651-2227&rft_id=info:doi/10.1111/j.1651-2227.1998.tb00934.x&rft_dat=%3Cproquest_cross%3E70118479%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70118479&rft_id=info:pmid/9846928&rfr_iscdi=true