Multiple carboxylase deficiency
id:
multiple-carboxylase-deficiency-263-16817678
title:
Multiple carboxylase deficiency
text:
Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes. The deficiency can be in biotinidase or holocarboxylase synthetase. These conditions respond to biotin. Forms include: Holocarboxylase synthetase deficiency - neonatal;
Biotinidase deficiency - late onset; If left untreated, the symptoms can include feeding problems, decreased body tone, generalized red rash with skin exfoliation and baldness, failure to thrive, seizure, coma, development
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Multiple_carboxylase_deficiency
date created:
date modified:
2024-04-15T07:13:37Z
main entity:
{"identifier":"Q6934914","url":"https://www.wikidata.org/entity/Q6934914"}
image:
fields total:
13
integrity:
14