Meet Whitney (10178)
Whitney is tall, standing at 6’3” and has a lean, muscular build. He maintains his physique with regular cardio and weight training. Whitney has a very “boy next door” look with blonde hair he keeps short and styled and ocean blue eyes. His eyes really stand out against his tan complexion. Whitney is always smiling revealing full, pink lips and straight, white teeth. All of these attributes make Whitney a very cute young man.
Whitney is a very friendly, personable, happy and sweet young man. He is always eager to engage in conversations with the staff and is very easy to talk to. He shows a genuine interest in those around him and has a very caring nature about him. Whitney is also very dedicated in his studies. He is pursuing a degree in Marketing. Whitney enjoys keeping busy in his free time playing golf and soccer. He is also very close with his family and enjoys being a brother and uncle and spends as much time with his family as possible, and proudly shows off pictures of his nieces and nephews whenever he gets the chance. Whitney is a great combination of looks, brains and personality and we’re enjoy having him as part of the donor program.
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Meet Whitney (10178)
Whitney is tall, standing at 6’3” and has a lean, muscular build. He maintains his physique with regular cardio and weight training. Whitney has a very “boy next door” look with blonde hair he keeps short and styled and ocean blue eyes. His eyes really stand out against his tan complexion. Whitney is always smiling revealing full, pink lips and straight, white teeth. All of these attributes make Whitney a very cute young man.
Whitney is a very friendly, personable, happy and sweet young man. He is always eager to engage in conversations with the staff and is very easy to talk to. He shows a genuine interest in those around him and has a very caring nature about him. Whitney is also very dedicated in his studies. He is pursuing a degree in Marketing. Whitney enjoys keeping busy in his free time playing golf and soccer. He is also very close with his family and enjoys being a brother and uncle and spends as much time with his family as possible, and proudly shows off pictures of his nieces and nephews whenever he gets the chance. Whitney is a great combination of looks, brains and personality and we’re enjoy having him as part of the donor program.
Blue
Blonde
191
86
A Rh+
-
Caucasian, Dutch, Norwegian
No
B.A. Marketing / Student
Yes
Counsyl Universal Panel minus x-linked conditions (at least 102 conditions)
-
- No disease causing mutations detected
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- Spinal Muscular Atrophy : Copy number 2
-
- Karyotyping
- Cystic Fibrosis
- ABCC8-related Hyperinsulinism
- Achromatopsia
- Alkaptonuria
- Alpha-1 Antitrypsin Deficiency
- Alpha-mannosidosis
- Alpha Thalassemia
- Andermann Syndrome
- 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
- Factor XI 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
- Glycogen Storage Disease Type V
- GRACILE Syndrome
- Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
- Hereditary Fructose Intolerance
- Hereditary Thymine-uraciluria
- 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 1B
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic Leukoencephalopathy With Subcortical Cysts
- Metachromatic Leukodystrophy
- Mucolipidosis IV
- 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
- Pseudocholinesterase Deficiency
- Pycnodysostosis
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Segawa Syndrome
- Short Chain Acyl-CoA Dehydrogenase Deficiency
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- Sulfate Transporter-related Osteochondrodysplasia
- 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
- Nephrotic Syndrome (NPHS2-Related) / Steroid-Resistant Nephrotic Syndr