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Multiple carboxylase deficiency
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From Wikipedia, the free encyclopedia
Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes.
The deficiency can be in biotinidaseorholocarboxylase synthetase.[1]
These conditions respond to biotin.[2]
Forms include:
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, developmental delay, foul smelling urine, lactic acidosis, and high levels of ketones and ammonia in the blood.
References[edit]
External links[edit]
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B7 Biotin/MCD |
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Other B |
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Other vitamin |
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Nonvitamin cofactor |
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Retrieved from "https://en.wikipedia.org/w/index.php?title=Multiple_carboxylase_deficiency&oldid=1219017814"
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●Vitamin, coenzyme, and cofactor metabolism disorders
●Endocrine, nutritional and metabolic disease stubs
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