Hi all
I had a CVS on Friday after two nuchal scans and bloods gave me high risk for Edwards Patau and Downs. Now anxiously awaiting the results...
I've been told by the hospital that the CVS tissue will only be analysed for those three conditions. They won't do a full karyotype study to look for any other chromosomal disorders, due to resource constraints.
Has anyone else been told this after a CVS or amnio? Did anyone manage to persuade their hospital to do the full karyotype study?
I guess the results on those 3 syndromes are the most important since they are the most common, but I can't help but feel that after taking the risk of having a CVS I would like them to look for everything they can!