Congenital Adrenal Hyperplasia (21 Hydroxylase Deficiency) MLPA

TEST CODE MG01610
TEST NAME Congenital Adrenal Hyperplasia (21 Hydroxylase Deficiency) MLPA
RELATED GENE CYP21A2,CYP21A1P,TNXB,ATF6B
SYNONYMOUS CYP21A2,CYP21A1P,TNXB,ATF6B
OMIM
HEREDITY
CLINICAL AREA Congenital Adrenal Hyperplasia is an Autosomal Recessively inherited disease. Mutations in the CFTR, ASZ1 and CTTNBP2 genes have been associated with the disease. This test screens deletion/duplication type mutations in disease-related genes with the MLPA method.
METHOD MLPA
SAMPLE TYPE Blood with EDTA
QUANTITY 3 mL
TAT 40 DAYS

ORDER OPTIONS AND PRICING

Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services