Meet Leopold (9647) – Open ID Donor.Back to Donor Search
- Eyes: Brown
- Hair: Dark Brown
- Height: 6'06"
- Weight (lbs): 220
- Blood: B Rh+
- CMV: -
- Ethnicity: Austrian, Caucasian, German, Irish, Latvian, Scottish
- Jewish Ancestry: No
- Education/Occupation: B.A. Political Science, J.D. / Lawyer
- Live Birth / Pregnancy Confirmed: Yes
- Extended Testing: Yes
- Genetically tested, and found to be negative, for: View
Leopold is incredibly tall and handsome. He has a chiseled jaw and strong masculine cheekbones. He has a flawless complexion that tans to a soft brown. Leopold has an impeccable smile and symmetrical features. He dresses well in button down shirts and khaki’s with a smart leather jacket over top.
Leopold is quite athletic and was on the U.S. national rowing team, narrowly missing his place on the U.S. Olympic team. He is incredibly intelligent and is finishing up his Law degree. Leopold is very driven and focused with a natural talent for sports and academia. He is outgoing, friendly, and enjoys meeting new people. Leopold is well rounded and quite an exceptional individual. We highly recommend Leopold and think he would make a wonderful donor for your family!
Over the years, we have expanded our genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. All donors have undergone genetic testing for Cystic Fibrosis, Spinal Muscular Atrophy and Karyotyping. However, many donors have had more extensive testing performed.
This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition please contact us, and we will provide a copy of the donor's test reports to your physician and/or genetic counselor.
|Karyotyping||Normal Male Karyoptype, 46XY|
|phenylalanine hydroxylase deficiency||Non-Carrier|
|spinal muscular atrophy||No disease-causing mutations detected (2 copies or more)|