Biotinidase Deficiency Biotinidase deficiency is an autosomal recessive inherited disorder that results in the inability to process the vitamin biotin in the normal way. Early symptoms of biotinidase deficiency generally - Multiple carboxylase deficiency - Document - PDFSEARCH.IO

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	Biotinidase Deficiency Biotinidase deficiency is an autosomal recessive inherited disorder that results in the inability to process the vitamin biotin in the normal way. Early symptoms of biotinidase deficiency generally Add to Reading List Document Date: 2011-11-10 05:37:29 Open Document File Size: 13,40 KB Share Result on Facebook MedicalCondition autosomal recessive inherited disorder / hypotonia / untreated biotinidase deficiency / Biotinidase Deficiency Biotinidase deficiency / metabolic acidosis / biotinidase deficiency / sudden infant death syndrome / coma / skin rash / disorder / seizures / / / Position Metabolic Specialist / / SocialTag Biotinidase deficiency Biotinidase Biotin Newborn screening Multiple carboxylase deficiency Holocarboxylase synthetase deficiency Health Genetics Genetic genealogy

Biotinidase Deficiency Biotinidase deficiency is an autosomal recessive inherited disorder that results in the inability to process the vitamin biotin in the normal way. Early symptoms of biotinidase deficiency generallyAdd to Reading List