Meet Aldo (9938) – Open ID Donor.

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Aldo has a lean, defined build; a result of his regular cardio and participation in a variety of recreational sports. He has straight brown hair that is complemented by stunning blue/green eyes. Aldo usually has a beard that is kept trimmed short, but will occasionally shave to reveal a clean, clear complexion. Aldo is very friendly, but has a sweet, somewhat shy smile full of straight white teeth.

Aldo is incredibly compassionate and caring. He is passionate about the environment and well-being of future generations. He currently works with children and hopes to have a future working in the field of environmental science, putting his degree to good use. Aldo is also athletic, playing a variety of sports recreationally, and can read music and play the piano. He can be quiet, but once comfortable Aldo is funny and intelligent, having thoughtful and engaging conversation and we believe he is a wonderful person and great 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