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genetic testing for PHA

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I confirmed Congenital Primary Hyperaldosteonism via AVS and have bilateral

adrenal hyperplasia and myofibrous dysplasia of both renal (left and right

kidney) arteries.

During 6 years of therapy I have had 2 lacunar infarcts.

The medical literature has many references to genetic testing.

My questions are: Why have the genetic testing done? And, would results of the

testing influence my therapy?

I live in Australia and the topic of genetic testing has never been raised by

the docs. Anyway it costs somewhere around $6,000 to have it done.

Any info would be helpful.

cheers,

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