Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
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Price: $950
|
Price: $750
|
Price: $1600
|
CPT: 81406
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CPT: 81405
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CPT: 81406
81405
|
Propionic acidemia is an autosomal recessive inborn error of metabolism. The disease is clinically very heterogeneous and characterized by metabolic ketoacidosis, vomiting, lethargy, and hypotonia. It is caused by a deficiency of propionyl-CoA carboxylase, an enzyme involved in the catabolism of branched chain amino acids, odd-numbered chain length fatty acids, and cholesterol. The enzyme is composed of α and β subunits which are encoded by the PCCA and PCCB genes, respectively. Mutations in either gene can cause propionic acidemia.
Type E
4 weeks or less