Question 1

Purpose of the Screening

Accepted Answer

Identifying if the fetus carries the G6PD genetic mutation. Enabling parents to plan proper medical care for the postnatal period. Avoiding triggers that cause hemolysis in the newborn immediately after birth.

Question 2

Who Should Get Tested?

Accepted Answer

Families with a confirmed history of G6PD deficiency. Mothers who have previously had children with the disorder. Cases where a genetic counselor recommends prenatal testing.

Question 3

Procedure Overview

Accepted Answer

Ultrasound is used to precisely locate the fetus and placenta. A thin needle is inserted through the abdomen to collect amniotic fluid. The sample is sent to a genetic lab for DNA analysis of specific mutations.

Ensure Your Baby's Genetic Health - Prenatal G6PD Deficiency Screening