https://wiki.tiffa.net/w/index.php?action=history&feed=atom&title=Translations%3ABiotin%2F23%2FenTranslations:Biotin/23/en - Revision history2026-09-14T04:39:16ZRevision history for this page on the wikiMediaWiki 1.43.0https://wiki.tiffa.net/w/index.php?title=Translations:Biotin/23/en&diff=134593&oldid=prevFuzzyBot: Importing a new version from external source2024-04-04T07:25:26Z<p>Importing a new version from external source</p>
<p><b>New page</b></p><div>Aside from inadequate dietary intake (rare), deficiency of biotin can be caused by a genetic disorder that affects biotin metabolism. The most common among these is [[biotinidase deficiency]]. Low activity of this enzyme causes a failure to recycle biotin from [[biocytin]]. Rarer are carboxylase and biotin transporter deficiences. Neonatal screening for biotinidase deficiency started in the United States in 1984, with many countries now also testing for this genetic disorder at birth. Treatment is lifelong dietary supplement with biotin. If biotinidase deficiency goes untreated, it can be fatal.</div>FuzzyBot