Meet Arjun (12074) – Open ID Donor – New Donor!.

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Arjun has an incredibly sweet and soft spoken nature. Every time he is in our office, Arjun personally greets everyone he sees with a friendly smile and a warm hello. Arjun is very handsome- he has a beautiful medium complexion that pairs well with his large, deep brown eyes and thick dark brown hair. He has a trim oval face with a square jawline, thick dark eyebrows, and an amazing, full smile. He stands tall at 6’2 and sports a fit and lean frame. Arjun loves to stay in shape and keeps fit by playing handball.

Arjun was a Dentist in India, and now living in the states, is studying to become a certified dentist here as well. He is extremely smart and well-spoken, which comes across the moment you meet him. Arjun’s striking good looks and endearing personality make him an excellent 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