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...
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Veröffentlicht in: | Acta Paediatrica 1998-11, Vol.87 (11), p.1205-1207 |
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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 |
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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. 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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> |
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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 |
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