I have just learned about CAH so please forgive me if
this is a stupid question. We are planning a family
and so gathering information about any hereditary
medical conditions that run in our families. There
was a female family member born in about 1928 who was
first thought to be male, given a boy's name, but soon
was found to be female. That's all I know. This girl
grew up, had children and leads a healthy, normal
life. She has not told family members that she suffers
from CAH or any hereditary medical condition. We do
not feel comfortable asking her about it. Are we crazy
to suspect the CAH gene? Or would it be prudent to
get genetic counselling on this issue? Is it an easy
test?
Thanks!

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