Meet Jude (12044) – Open ID Donor.

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Jude Staff Impression

Jude is slender and very tall, has long arms and legs, and stays in great shape physically without looking overly athletic. He has an incredibly handsome face- big brown/green eyes, long nose, wide smile, and an attractive, square jaw line. He has fair to medium skin and neatly cut brown hair. His look is always very professional and polished.

Jude has a humble and unassuming attitude while in the office, but happens to be one of the most brilliant and accomplished young donors we have. He had an illustrious academic career, not only earning his M.D., but also an MBA and MS in Biomedical Engineering. He is currently a resident physician and researcher, and somehow still makes time to enjoy pursuing a variety of hobbies and interests, including playing the piano, reading, skiing, long distance running, learning new languages, and traveling. We are more than thrilled to have Jude in our donor program!



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