![B vitamins / Biotinidase deficiency / Genes / Biotinidase / Biotin / Multiple carboxylase deficiency / Medical genetics / 3-Methylcrotonyl-CoA carboxylase deficiency / Holocarboxylase synthetase deficiency / Medicine / Genetics / Health B vitamins / Biotinidase deficiency / Genes / Biotinidase / Biotin / Multiple carboxylase deficiency / Medical genetics / 3-Methylcrotonyl-CoA carboxylase deficiency / Holocarboxylase synthetase deficiency / Medicine / Genetics / Health](https://www.pdfsearch.io/img/e442c87465c6a5c11679fd5de51c9a38.jpg)
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Company 2888 Shaganappi Trail N.W. Calgary AB / St. N.W. Edmonton AB / / Country Canada / / Facility Children’s Hospital / Edmonton Medical Genetics Clinic / Inherited Metabolic Disorders Clinic / Medical Sciences Building / / / IndustryTerm treatment of BlOT before symptoms / / MedicalCondition lethargy / organic acid disorders / acid disorders / metabolic diseases / seizures / late-onset multiple carboxylase deficiency BlOT / Biotinidase Deficiency / organic acid disorder / skin rash / partial deficiency / minor illness / partial biotinidase deficiency / / Organization Inherited Metabolic Disorders Clinic Alberta Children’s Hospital / / / Position genetic metabolic specialist / / URL www.albertahealthservices.ca/newbornscreening.asp / /
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