Meet Marlon (12220)
The best way to describe Marlon is classically handsome with a charming personality. He is clean-cut with thick, wavy hair, gorgeous tan skin, strong brows, and a full-lipped smile that frames straight, white teeth. Long limbs, broad shoulders, and a muscular build make Marlon look like a natural athlete; he was an All-American Rugby player for two seasons who also participated in many other team and individual sports. The cold days of winter don’t slow him down as he looks forward to heading up to the mountains for his favorite pastime, skiing.
Marlon is a warm, loyal, and humorous guy who greatly values spending quality time with his family and loved ones. He is happy to be making his family proud while he pursues his goal of completing business school. His strong work ethic, optimism, and generosity make Marlon a fantastic guy!
You must be logged in to proceed.
1 Family Slots are currently available for purchase.
Meet Marlon (12220)
The best way to describe Marlon is classically handsome with a charming personality. He is clean-cut with thick, wavy hair, gorgeous tan skin, strong brows, and a full-lipped smile that frames straight, white teeth. Long limbs, broad shoulders, and a muscular build make Marlon look like a natural athlete; he was an All-American Rugby player for two seasons who also participated in many other team and individual sports. The cold days of winter don’t slow him down as he looks forward to heading up to the mountains for his favorite pastime, skiing.
Marlon is a warm, loyal, and humorous guy who greatly values spending quality time with his family and loved ones. He is happy to be making his family proud while he pursues his goal of completing business school. His strong work ethic, optimism, and generosity make Marlon a fantastic guy!
Green
Brown
196
95
A Rh+
-
Caucasian, German, Lebanese, Scottish
No
B.A. Business / Student
Yes
Counsyl Universal Panel minus x-linked conditions (at least 102 conditions)
-
- 21-hydroxylase Deficient Congenital Adrenal Hyperplasia : Carrier
- Autosomal Recessive Primary Microcephaly 8 : Carrier
-
- 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
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Disorder Of Glycosylation Type Ib
- Congenital Finnish Nephrosis
- Costeff Optic Atrophy Syndrome
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydropyrimidine Dehydrogenase Deficiency
- Factor XI Deficiency
- Familial Dysautonomia
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Galactosemia
- 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
- 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
- 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
- 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
- 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
- COL4A3-related Alport Syndrome
- USH2A-related Disorders
- Nephrotic Syndrome (NPHS2-Related) / Steroid-Resistant Nephrotic Syndr