Carrier screening identifies healthy adults who carry a recessive gene change that could affect their children.
Most carriers are completely healthy and have no family history. Carrier screening is a blood test that looks for changes in genes linked to recessive conditions such as thalassaemia, spinal muscular atrophy, cystic fibrosis and many others.
It is most valuable before pregnancy, when the full range of reproductive options is still available.
This page is general information and is not a substitute for a consultation. Every pregnancy is assessed individually.
Most pregnancy complications are not anyone's fault. Understanding the underlying cause is the first step towards answers.
Recurrence risk depends entirely on the underlying mechanism — which is why finding the cause matters so much.
Genetic testing is not routine for everyone. It is indicated when the result would change diagnosis, management or future planning.
Consultations at Apollo Cradle, Apollo Fertility, AIFMRG and Epic International, Hyderabad.