Meet Malcolm (9681) – Open ID Donor.

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Malcolm has entrancing eyes that glimmer with kindness. He is adorable and has a sweet shy smile. His skin tone is fair and has a slightly ruddy tinge. Malcolm has a cute button nose that compliments his delicate features well. He has a thin build and lifts weights to maintain his muscular definition. He dresses in dark t-shirts and jeans.

Malcolm can be quiet and introspective. He has a tranquil demeanor and is very laid back. Malcolm is a proud nerd and loves to play dungeons and dragons with his friends as it allows him a great opportunity to be creative. He is also an avid convention go-er and likes to collect sci-fi items. We asked Malcolm to describe some of his strong sides and he said, “I can prioritize very well, people recognize that I am well-organized. I am punctual, people think of me when they need someone reliable.” We also think his good will and sweetness should be touted as a strong side!

 

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
achromatopsia Non-Carrier
alkaptonuria Non-Carrier
alpha-1 antitrypsin deficiency Non-Carrier
alpha-mannosidosis Non-Carrier
Andermann syndrome Non-Carrier
ARSACS Non-Carrier
aspartylglycosaminuria Non-Carrier
ataxia with vitamin E deficiency Non-Carrier
ataxia-telangiectasia Non-Carrier
autosomal recessive polycystic kidney disease Non-Carrier
Bardet-Biedl syndrome, BBS1-related Non-Carrier
Bardet-Biedl syndrome, BBS10-related Non-Carrier
Biotinidase Deficiency Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
carnitine palmitoyltransferase 1A deficiency Non-Carrier
carnitine palmitoyltransferase II deficiency Non-Carrier
cartilage-hair hypoplasia Non-Carrier
choroideremia Non-Carrier
citrullinemia type 1 Non-Carrier
CLN3-related neuronal ceroid lipofuscinosis Non-Carrier
CLN5-related neuronal ceroid lipofuscinosis Non-Carrier
Cohen syndrome Non-Carrier
congenital disorder of glycosylation type 1a Non-Carrier
congenital disorder of glycosylation type 1b Non-Carrier
congenital Finnish nephrosis Non-Carrier
Costeff optic atrophy syndrome Non-Carrier
cystic fibrosis Non-Carrier
cystinosis Non-Carrier
D-bifunctional protein deficiency Non-Carrier
factor XI deficiency Non-Carrier
familial dysautonomia Non-Carrier
familial Mediterranean fever Non-Carrier
Fanconi anemia type C Non-Carrier
galactosemia Non-Carrier
Gaucher disease Non-Carrier
GJB2-related DFNB1 nonsyndromic hearing loss and deafness Non-Carrier
glutaric acidemia type 1 Non-Carrier
glycogen storage disease type Ia Non-Carrier
glycogen storage disease type Ib Non-Carrier
glycogen storage disease type III Non-Carrier
glycogen storage disease type V Non-Carrier
GRACILE syndrome 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
hereditary fructose intolerance Non-Carrier
hereditary thymine-uraciluria Non-Carrier
Herlitz junctional epidermolysis bullosa, LAMA3-related Non-Carrier
Herlitz junctional epidermolysis bullosa, LAMB3-related Non-Carrier
Herlitz junctional epidermolysis bullosa, LAMC2-related Non-Carrier
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
homocystinuria caused by cystathionine beta-synthase deficiency Non-Carrier
Hurler syndrome Non-Carrier
hypophosphatasia, autosomal recessive Non-Carrier
inclusion body myopathy 2 Non-Carrier
isovaleric acidemia Non-Carrier
Joubert syndrome 2 Non-Carrier
Krabbe disease Non-Carrier
limb-girdle muscular dystrophy type 2D Non-Carrier
limb-girdle muscular dystrophy type 2E Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
medium chain acyl-CoA dehydrogenase deficiency Non-Carrier
megalencephalic leukoencephalopathy with subcortical cysts Non-Carrier
metachromatic leukodystrophy Non-Carrier
mucolipidosis IV Non-Carrier
muscle-eye-brain disease Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease type C Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
Nijmegen breakage syndrome Non-Carrier
Northern epilepsy Non-Carrier
Pendred syndrome Non-Carrier
PEX1-related Zellweger Syndrome Spectrum Non-Carrier
phenylalanine hydroxylase deficiency Non-Carrier
polyglandular autoimmune syndrome type 1 Non-Carrier
Pompe disease Non-Carrier
PPT1-related neuronal ceroid lipofuscinosis Non-Carrier
primary carnitine deficiency Non-Carrier
primary hyperoxaluria type 1 Non-Carrier
primary hyperoxaluria type 2 Non-Carrier
PROP1-related combined pituitary hormone deficiency Non-Carrier
pseudocholinesterase deficiency Non-Carrier
pycnodysostosis Non-Carrier
rhizomelic chondrodysplasia punctata type 1 Non-Carrier
Salla disease Non-Carrier
Segawa syndrome Non-Carrier
short chain acyl-CoA dehydrogenase deficiency Non-Carrier
Sjogren-Larsson syndrome Non-Carrier
Smith-Lemli-Opitz syndrome Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies)
steroid-resistant nephrotic syndrome Non-Carrier
sulfate transporter-related osteochondrodysplasia Non-Carrier
TPP1-related neuronal ceroid lipofuscinosis Non-Carrier
tyrosinemia type 1 Non-Carrier
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
very long chain acyl-CoA dehydrogenase deficiency Non-Carrier
Wilson disease Non-Carrier
x-linked juvenile retinoschisis Non-Carrier