Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
---|---|---|
Price: $950
|
Price: $750
|
Price: $1600
|
CPT: 81406
|
CPT: 81405
|
CPT: 81406
81405
|
Phenylketonuria (PKU) is an autosomal recessive inborn error of metabolism resulting from a deficiency of phenylalanine hydroxylase (PAH), an enzyme that catalyzes the conversion of phenylalanine to tyrosine. If undiagnosed and untreated, PKU can result in mental retardation, seizures and other serious medical problems.
Type E
4 weeks or less