Meet Pavl (9983) – Open ID Donor.

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Pavl has a beautiful, smooth, olive complexion. He has brown eyes and thick, dark brown hair. He has very symmetrical facial features including a smile with straight, white teeth. Pavl exercises regularly, mostly through sports, to maintain an athletic physique. All of these features make Pavl a very handsome donor.

Pavl is very smart and always ready to engage in thoughtful conversation. He has strong opinions that are based largely on his views and personal experience. Pavl loves to travel and has had the opportunity to visit many different countries all over the world. Each place he visits, he really strives to capture the history and culture. Pavl is also athletic and plays on his college water polo team and on a variety of intramural sports teams. He is competitive but at the same time laid back and outgoing, making it easy for him to make friends. We believe that Pavl’s drive to succeed and his great sense of humor make him a wonderful donor.

Genetic Testing

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
ABCC8-related hyperinsulinism Non-Carrier
alpha thalassemia Non-Carrier
ARSACS Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cystic fibrosis Non-Carrier
familial dysautonomia Non-Carrier
Fanconi anemia type C Non-Carrier
Gaucher disease Non-Carrier
glycogen storage disease type Ia Non-Carrier
Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease) No disease-causing mutations detected; normal complete blood count and hemoglobin analysis
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
Joubert syndrome 2 Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
mucolipidosis IV Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
Walker-Warburg syndrome Non-Carrier