Multiple carboxylase deficiency: Difference between revisions
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{{Infobox disease | | {{Infobox disease | | ||
Name = Multiple carboxylase deficiency | | Name = Multiple carboxylase deficiency | | ||
Latest revision as of 14:39, 16 December 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
| Multiple carboxylase deficiency | |
| Classification and external resources | |
| MeSH | D009100 |
|---|---|
Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes.
The deficiency can be in biotinidase or holocarboxylase synthetase.[1]
These conditions respond to biotin.[2]
Forms include:
- Holocarboxylase synthetase deficiency - neonatal;
- Biotinidase deficiency - late onset;
If left untreated, the symptoms can include feeding problems, hypotonia, generalised erythematous rash with skin exfoliation and alopecia, failure to thrive, seizure, coma, developmental delay, foul smelling urine, metabolic acidosis, ketosis and hyperammonemia.
References
External links
Template:Metabolic disorders of vitamins, coenzymes, and cofactors