Multiple Carboxylase Deficiency Organic Acidemia as a Cause of Infantile Seizures.
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DOI: 10.29271/jcpsp.2021.01.95
Abstract: Multiple carboxylase deficiency organic Acidemia is a rare inherited metabolic disorder. It is autosomal recessive disorder of two types: Holocarboxylase deficiency and Biotinidase deficiency. It is the metabolic disorder resulting from deficiency of biotin as… read more here.
Keywords: multiple carboxylase; organic acidemia; carboxylase; deficiency organic ... See more keywords