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NOVA™ METABOLIC DISORDER DISEASE (48+3)

Genetic screening for 48 inherited metabolic disorders (IMDs) + 3 congenital diseases (CAH, CH & G6PDD) for newborns.

Remarks: This product is available, kindly contact us for more in details. Thank you.

PRODUCT DESCRIPTION

Description

Suitable for
· Newborn who is suspected with a metabolic abnormality

Turn-Around Time (TAT)
· 10 Working Days

Sample Requirement
· 3 dried blood spots
*Blood collection from 48 hours to 7 days after birth and fully breastfeed for 6 times