Holocarboxylase synthetase deficiency
id:
holocarboxylase-synthetase-deficiency-266-4021164
title:
Holocarboxylase synthetase deficiency
text:
Holocarboxylase synthetase deficiency is an inherited metabolic disorder in which the body is unable to use the vitamin biotin effectively. This disorder is classified as a multiple carboxylase deficiency, a group of disorders characterized by impaired activity of certain enzymes that depend on biotin. Symptoms are very similar to biotinidase deficiency and treatment – large doses of biotin – is also the same.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Holocarboxylase_synthetase_deficiency
date created:
date modified:
2021-10-05T14:46:47Z
main entity:
{"identifier":"Q5883885","url":"https://www.wikidata.org/entity/Q5883885"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/8/85/Biotin_structure.svg","width":1200,"height":670}
fields total:
13
integrity:
15