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Meet Garston
Active
Family Slot Donor
Garston is charming, inquisitive, and profound with his words. He has beautiful hazel eyes and a broad smile. We enjoy having conversations with him, as he has a calming personality, yet is still very personable and social. Garston works as a mechanic in the U.S. Navy and has always been proficient in math. He is bilingual, as he is fluent in German and one day hopes to travel to Germany to be able to interact with others who speak the language. In his free time, Garston enjoys playing the ukulele, singing, and writing, which did not come as a surprise to us; Garston is a hardworking person, with a creative soul and we are very thankful to have him in our program!
Eyes
Brown/Green
Hair
Light Brown
Height
178 cm
Weight
68 kg
Blood
O Rh+
CMV
-
Ethnicity
Caucasian, Czech, Eastern European, English, German, Welsh
Education/Occupation
Naval Nuclear Training & nursing school / Machinist Mate Nuclear
Live Birth/Pregnancy Confirmed
Yes
Genetic Carrier Screening Panel Completed by Donor
Counsyl Foresight Panel (at least 175 conditions)
Carrier Screening Results Positive For
No disease causing mutations detected
Karyotype Result
Karyotyping: 46,XY
Results with No Disease Causing Mutations
- Cystic fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related hyperinsulinism
- Alpha-Mannosidosis
- Alpha Thalassemia
- Andermann syndrome
- Argininosuccinic Aciduria
- ARSACS
- Aspartylglycosaminuria
- Ataxia with vitamin E deficiency
- Ataxia-telangiectasia
- Autosomal recessive polycystic kidney disease
- Bardet-Biedl syndrome, BBS1-related
- Bardet-Biedl syndrome, BBS10-related
- Biotinidase Deficiency
- Bloom syndrome
- Canavan disease
- Carnitine palmitoyltransferase IA deficiency
- Carnitine palmitoyltransferase II deficiency
- Cartilage-hair hypoplasia
- Citrullinemia type 1
- CLN3-related neuronal ceroid lipofuscinosis
- CLN5-related neuronal ceroid lipofuscinosis
- Cohen syndrome
- 21-hydroxylase deficient congenital adrenal hyperplasia
- Congenital disorder of glycosylation type Ia
- Congenital disorder of glycosylation type Ib
- Congenital Finnish nephrosis
- Costeff optic atrophy syndrome
- Cystinosis
- D-bifunctional protein deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Familial dysautonomia
- Familial Mediterranean fever
- Fanconi anemia type C
- Galactosemia
- Gaucher disease
- GJB2-related DFNB1 nonsyndromic hearing loss and deafness
- Glutaric acidemia type 1
- Glycogen storage disease type Ia
- Glycogen storage disease type Ib
- Glycogen storage disease type II
- Glycogen storage disease type III
- GRACILE syndrome
- Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease)
- Hereditary fructose intolerance
- HMG-CoA Lyase Deficiency
- Herlitz junctional epidermolysis bullosa, LAMB3-related
- Herlitz junctional epidermolysis bullosa, LAMC2-related
- Hexosaminidase A deficiency (including Tay-Sachs disease)
- Homocystinuria caused by cystathionine beta-synthase deficiency
- Hurler syndrome
- Hypophosphatasia, autosomal recessive
- Inclusion body myopathy 2
- Isovaleric acidemia
- Joubert syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Krabbe disease
- Limb-girdle muscular dystrophy type 2D
- Limb-girdle muscular dystrophy type 2E
- Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- Maple syrup urine disease type 1A
- Maple syrup urine disease type 1B
- Medium chain acyl-CoA dehydrogenase deficiency
- Megalencephalic leukoencephalopathy with subcortical cysts
- Metachromatic leukodystrophy
- Methylmalonic Acidemia MUT-related
- Methylmalonic Aciduria and Homocystinuria Type cbIC
- Mucolipidosis IV
- Mucopolysaccharidosis Type I
- Muscle-eye-brain disease
- NEB-related nemaline myopathy
- Niemann-Pick disease type C
- Niemann-Pick disease, SMPD1-associated
- Nijmegen breakage syndrome
- Northern epilepsy
- Pendred syndrome
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine hydroxylase deficiency
- Polyglandular autoimmune syndrome type 1
- PPT1-related neuronal ceroid lipofuscinosis
- Primary carnitine deficiency
- Primary hyperoxaluria type 1
- Primary hyperoxaluria type 2
- PROP1-related combined pituitary hormone deficiency
- Pycnodysostosis
- Rhizomelic chondrodysplasia punctata type 1
- Salla disease
- Sandhoff Disease
- Segawa syndrome
- Short chain acyl-CoA dehydrogenase deficiency
- Sjogren-Larsson syndrome
- Smith-Lemli-Opitz syndrome
- Sulfate transporter-related osteochondrodysplasia (SLC26A2)
- TPP1-related neuronal ceroid lipofuscinosis
- Tyrosinemia type I
- Usher syndrome type 1F
- Usher syndrome type 3
- Very long chain acyl-CoA dehydrogenase deficiency
- Walker-Warburg syndrome
- Wilson disease
- Maple syrup urine disease type II
- 6-pyruvoyl-tetrahydropterin synthase deficiency
- 11-beta-hydroxylase-deficient congenital adrenal hyperplasia
- Alstrom syndrome
- AMT-related glycine encephalopathy
- Argininemia
- ATP7A-related disorders
- Autosomal recessive osteopetrosis type 1
- Bardet-Biedl syndrome, BBS12-related
- Bardet-Biedl syndrome, BBS2-related
- Calpainopathy
- Carbamoylphosphate synthetase I deficiency
- Cerebrotendinous xanthomatosis
- CLN6-related neuronal ceroid lipofuscinosis
- COL4A3-related Alport syndrome
- COL4A4-related Alport syndrome
- Congenital disorder of glycosylation type Ic
- Delta-sarcoglycanopathy
- Dysferlinopathy
- Dystrophinopathy (including Duchenne/Becker muscular dystrophy)
- ERCC6-related disorders
- ERCC8-related disorders
- EVC-related Ellis-van Creveld syndrome
- EVC2-related Ellis-van Creveld syndrome
- Fabry disease
- Fanconi anemia complementation group A
- FKRP-related disorders
- Galactokinase deficiency
- Gamma-sarcoglycanopathy
- GLB1-related disorders
- GLDC-related glycine encephalopathy
- GNPTAB-related disorders
- Hydrolethalus syndrome
- KCNJ11-related familial hyperinsulinism
- LAMA2-related muscular dystrophy
- Leigh syndrome, French-Canadian type
- Lipoid congenital adrenal hyperplasia
- Lysosomal acid lipase deficiency
- Methylmalonic acidemia, cblA type
- Methylmalonic acidemia, cblB type
- MKS1-related disorders
- Mucolipidosis III gamma
- Mucopolysaccharidosis type II
- Mucopolysaccharidosis type IIIA
- Mucopolysaccharidosis type IIIB
- Mucopolysaccharidosis type IIIC
- MYO7A-related disorders
- Niemann-Pick disease type C2
- Ornithine transcarbamylase deficiency
- PCCA-related propionic acidemia
- PCCB-related propionic acidemia
- Peroxisome biogenesis disorder type 3
- Peroxisome biogenesis disorder type 4
- Peroxisome biogenesis disorder type 5
- Peroxisome biogenesis disorder type 6
- Primary hyperoxaluria type 3
- Pyruvate carboxylase deficiency
- RTEL1-related disorders
- Spastic paraplegia type 15
- Spondylothoracic dysostosis
- TGM1-related autosomal recessive congenital ichthyosis
- Tyrosinemia type II
- USH1C-related disorders
- USH2A-related disorders
- X-linked adrenoleukodystrophy
- X-linked Alport syndrome
- X-linked congenital adrenal hypoplasia
- X-linked myotubular myopathy
- X-linked severe combined immunodeficiency
- Xeroderma pigmentosum group A
- Xeroderma pigmentosum group C
- Nephrotic Syndrome (NPHS2-Related)
- Odonto-Onycho-Dermal Dysplasia / Schopf-Schulz-Passarge Syndrome
- Lysinuric Protein Intolerance
