Holocarboxylase synthetase deficiency

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Name:
Holocarboxylase synthetase deficiency
Description:
A rare, early-onset and life-threatening, multiple carboxylase deficiency that when left untreated, is characterized by vomiting, tachypnea, irritability, lethargy, exfoliative dermatitis, and seizures that can worsen to coma and death.
ORPHAcode:
79242
Synonyms:
Early-onset multiple carboxylase deficiency
Neonatal multiple carboxylase deficiency
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14