This donor completed additional genetic carrier screening that provides helpful information you can use for your family building journey!  Donor PC 1120 was screened for 283 genetic conditions and was found to be a carrier for: 

• Bartter Syndrome, Type 4a;

• Non-syndromic Hearing Loss (GJB2-related); and

• Smith-Lemli-Opitz Syndrome.

Please see PC 1120’s test results and Additional Agreement for more information, and then simply sign the Additional Agreement when you have selected your donor. 

I understand this donor has had additional genetic testing and I have read the Additional Agreement.