To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Cerano (9650) – Open ID Donor
Trouvez un Donneur- Yeux : Vert
- Cheveux : Brun foncé
- Taille : 5'11"
- Poids (en livres) : 155
- Groupe sanguin : A Rh+
- CMV : -
- Origine ethnique : Caucasian, Greek
- Ascendance juive : Oui
- Éducation/profession : B.A. Sociology and Business/ Actor and Writer
- Grossesse confirmée : Oui
Résultats des tests génétiques
- Dépistage étendu : Non
- Transporteur pour :
- No disease causing mutations detected
- Résultats pour Karyotyping / Amyotrophie musculaire spinale :
- Amyotrophie musculaire spinale: Copy number 2
- Résultats sans maladie causant des mutations : Découvre
- Karyotyping
- Cystic Fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related Hyperinsulinism
- Alpha-1 Antitrypsin Deficiency
- Andermann Syndrome
- Argininosuccinic Aciduria
- ARSACS
- Aspartylglycosaminuria
- Ataxia-telangiectasia
- Autosomal Recessive Polycystic Kidney Disease
- Bardet-Biedl Syndrome, BBS1-related
- Bardet-Biedl Syndrome, BBS10-related
- Beta-Thalassemia
- Bloom Syndrome
- Canavan Disease
- Cartilage-hair Hypoplasia
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN5-related Neuronal Ceroid Lipofuscinosis
- CLN8-related Neuronal Ceroid Lipofuscinosis
- Cobalamin C Disease
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Finnish Nephrosis
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Dihydropyrimidine Dehydrogenase Deficiency
- Ethylmalonic Encephalopathy
- Familial Dysautonomia
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Galactosemia
- Gaucher Disease
- Glutaric Acidemia Type 1
- Glutathione Synthetase Deficiency
- Glycine Encephalopathy
- 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
- Holocarboxylase Synthetase Deficiency
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Hurler Syndrome
- Hyperoxaluria Type 1
- Hyperoxaluria Type 2
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Junctional Epidermolysis Bullosa, LAMB3-related
- Junctional Epidermolysis Bullosa, LAMC2-related
- Krabbe Disease
- Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- Leigh Syndrome
- Maple Syrup Urine Disease Type 1A
- Maple Syrup Urine Disease Type 1B
- Maple Syrup Urine Disease Type 3
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Metachromatic Leukodystrophy
- Methylmalonic Acidemia MMAA-related
- Methylmalonic Acidemia MMAB-related
- Methylmalonic Acidemia MUT-related
- Methylmalonic Aciduria And Homocystinuria Type CbIC
- Mucolipidosis IV
- Mucopolysaccharidosis Type I
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease Type A
- Niemann-Pick Disease Type B
- Niemann-Pick Disease Type C
- Nijmegen Breakage Syndrome
- Non-Ketonic Hyperglycinemia, GLDC-Related
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine Hydroxylase Deficiency
- PPT1-related Neuronal Ceroid Lipofuscinosis
- Primary Hyperoxaluria Type 1
- Primary Hyperoxaluria Type 2
- Propionic Acidemia, PCCA-Related
- Propionic Acidemia, PCCB-Related
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Sandhoff Disease
- Sickle Cell Disease
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- Sulfate Transporter-related Osteochondrodysplasia (SLC26A2)
- Tay-Sachs Disease (Counsyl)
- TPP1-related Neuronal Ceroid Lipofuscinosis
- Tyrosinemia Type I
- Usher Syndrome Type 1F
- Usher Syndrome Type 3
- Walker-Warburg Syndrome
- Wilson Disease
- Nephrotic Syndrome (NPHS1-Related)
- Nephrotic Syndrome (NPHS2-Related)
Description du Donneur
Cerano’s greek heritage is easy to see in his appearance. He has thick dark curls and a gorgeous olive skin tone. His complexion is flawless and he has a great smile. Cerano also has twin dimples on his cheeks! He has a thin build and remains very active. He dresses well in polo shirts and khaki’s.
Cerano likes to describe himself as a mix of extrovert and introvert. He can be quiet in some situations and very outgoing and sociable in others. He is genuine and sincere in his actions and words. Cerano is a deep thinker and creative. We asked Cerano what he was most proud of and he said, “I'm most proud that I have chosen a unique path in life. I pursue the things that are important to me. I don't work in a job that is meaningless to me. I continue to question; I continue to explore; I continue to learn; I continue to grow as a person. I'm proud that, despite all the challenges that come with this approach to life, I remain on this path. “ We love Cerano’s passion and enthusiasm for the world around him.