Potter’s Syndrome
Wednesday 6th January 2010 - 5:01 AMI’m starting to get a lot of hits on my website from people looking for information on bilateral renal agenesis. If you are a parent or family member of a baby diagnosed with bilateral renal agenesis (Potter’s Syndrome) then I strongly urge you to also visit this website. Dr Brophy and Dr Clarke are currently accepting families into their research study. It won’t cost you a cent to participate and they only need blood samples. Don’t worry if you don’t live in North America as they have enrolled families from around the world in the study and will give you a Fed-Ex account number to ship your samples to their lab. Their research study is currently the only study being done into bilateral renal agenesis.
