Biotinidase deficiency

Disease Export to PDF
Name:
Biotinidase deficiency
Description:
A late-onset form of multiple carboxylase deficiency, an inborn error of biotin metabolism that, if untreated, is characterized by seizures, breathing difficulties, hypotonia, skin rash, alopecia, hearing loss and delayed development.
ORPHAcode:
79241
Synonyms:
Juvenile-onset multiple carboxylase deficiency
Late-onset multiple carboxylase deficiency
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14