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Foetal screening of inherited disorders

 

Foetal screening of inherited disorders: examples of inherited disorders include cystic fibrosis, b-thalassaemia, spinal muscular atrophy, Huntington’s chorea and many others. If one or both parents are carriers of a mutation for a genetic disorder, the baby is at risk of being affected by that disorder. The risk varies depending on the syndrome. We can screen cells from the foetus to ascertain whether the baby will be affected or not. As well as cells from amniotic fluid or chorionic villus, we also require a sample of peripheral blood from both parents. (more information on inherited disorders).

 
   
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