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Hello group.

I just came across this group as I was searching for updated

information on blepharophimosis. My middle daugther (age 6) was

diagnoised with this condition shortly after birth. She has a local

surgeon and a surgeon also in Michigan. Her surgeon in Michigan has

completed two of the three reconstructive surgeries. My daugther will

have the third and final surgery this December. We are so excited

that the surgeries will finally be over for her soon. We visited with

a genetic counselor recently and discovered that there is only one

other person in our local area with Blepharophomosis. She is in her

thirties. It is nice to see that their is an online group available

for support.

If there are parents who recently received this diagnosis regarding

their child. E-mail me and I'll be happy to share any information I

have as well as our families experience.

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