Meet Arthur (9996) – Open ID Donor.

Back to Donor Search

Arthur is very attractive with light brown hair and beautiful green eyes. He keeps his hair short, but when it grows out you can see how wavy and thick it is. Arthur is very active; engaging in soccer, skateboarding, weightlifting and other activities on a regular basis. All these forms of exercise give him well-defined muscles. Arthur also has a very straight, white smile that he shows off whenever he comes into the office.

Arthur is incredibly sweet with a very mellow and laid back personality. He is a little shy and quiet at first, but will open up after a short period to display his truly relaxed and kind personality. Arthur is also athletic, and played a wide range of sports in high school. Aside from his good looks and athletic prowess, Arthur is also very sweet, sincere and has an amazingly close relationship with his family and happily acknowledges the hand they played in shaping the amazing young man he is today.

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