Variants in AKR1D1 and Infant Mortality: Should Bile Acid Screening be a Routine Part of Newborn Screening?

Jade Hudson1, Stephanie Hyunh1, Bojana Rakic2

  • 1Department of Medical Genetics and Provincial Medical Genetics Program, University of British Columbia and Women's Hospital of British Columbia, Vancouver, British Columbia, Canada.

Summary

Congenital Bile Acid Synthesis defect type 2 (CBAS2), caused by AKR1D1 variants, disrupts bile acid production. Early diagnosis and intervention are crucial to prevent severe outcomes like infant death.

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