Meet Abner (9873) – Open ID Donor.

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Abner is tall with large muscles from his athletic lifestyle and regular exercise. He enjoys playing a variety of sports and engaging in just about any outdoor activity. Abner has thick, wavy, dark brown hair and big green/brown eyes. He has an equally dark beard that he keeps short and neatly trimmed, hiding his small dimples. Abner has masculine features that make him a very handsome individual.

Abner is very athletic, intelligent and outgoing. He played sports at the Division I collegiate level but also has an artistic side, enjoying painting and ceramics. He has exceptional interpersonal skills and is quick to laugh and make those around him laugh and feel completely at ease. Abner is an amazing father and we love how family oriented he is. When asked why he wants to be a donor, Abner answered, “It’s a special thing to be a part of – science can be a wonderful thing.” Abner is a patriotic, strong, athletic and good-humored 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
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