Meet Barton (9934) – Open ID Donor.

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  • Eyes: Blue/Green
  • Hair: Dark Brown
  • Height: 6'00"
  • Weight (lbs): 170
  • Blood: O Rh-
  • CMV: +
  • Ethnicity: Caucasian, German, Irish
  • Jewish Ancestry: No
  • Education/Occupation: B.S. Civil Engineering / Student
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View

Barton has a very toned build, with well-defined muscles. He is naturally athletic and stays in shape through swimming, Kung Fu, and many body weight exercises, although he played a variety of sports when he was younger. Barton has thick brown hair, and gorgeous blue/green eyes that pop against his fair skin. He keeps his face clean shaven and his hair short. Barton is a very attractive young man whose looks only serve to augment his already stellar personality.

 

Barton is one of our sweetest and most genuine donors. He truly is an incredible young man with an extremely caring side coupled with natural athleticism and an acute intellect. He is currently pursuing a degree in engineering while doing everything he can to help others, including donating for us and also donating blood as often as he can. Barton has strong morals and is always trying to improve himself and those around him.

 

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