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C0123
Citrullinemia gene panel
Test Details: Citrullinemia is an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. This test analyzes genes that are associated with elevated citrulline on newborn screening (NBS) or plasma amino acids. This test may confirm a diagnosis and help in treatment and management decisions. Identification of a pathogenic variant would guide testing of at-risk family members.
Category
Genotyping and Genomics
Pre-test Information
No special preparation.
Report Delivery
30 working days
Gender
All
Organ
Multi-Organ
Citrullinemia gene panel
23500
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