RALLEE Certified Feline Genetic Testing Panel 1
$1,549.00
For symptoms involving: Hearing, Nervous System, Vision
RALLEE® Certified Feline Genetic Testing Panel 1
RALLEE® Certified Feline Genetic Testing Panel 1 includes genetic testing for diseases with symptoms involving hearing, nervous system, and vision that may be difficult to accurately diagnose clinically due to rarity or due to broad symptoms that are common to multiple diseases. Understanding the specific genetic cause for your cat’s symptoms allows your veterinarian to identify the best treatment possible, potentially including enrollment in experimental therapies.
Number of Alleles Tested: 30 |
|
Condition |
Gene(s) |
Alpha Mannosidosis | MAN2B1 |
Brachycephaly and Craniofacial Defects | ALX1 |
Congenital Glaucoma | LTBP2 |
Dihydropyrimidinase (DHP) | CPYS |
Erythrocyte Pyruvate Kinase Deficiency (PK Deficiency) | PKLR |
Glycogen Storage Disease Type IV (GSD IV) | GBE |
GM1 Gangliosidosis 1-5 | GLB1, GM2A, HEXB |
Hemophilia B 1, 2 | F9 |
Hypokalemic Periodic Paralysis | WNK4 |
Leber Congenital Amaurosis (or Retinal Pigment Epithelial Dystrophy) | AIPL |
Mucolipidosis II | GNPTAB |
Mucopolysaccharidosis VII 1, 2 | GUSB |
Neuronal Ceroid Lipofuscinosis Type 7 (CLN7) | MFSD8 |
Niemann-Pick Disease Type C1 (NPC1) 1, 2 | NPC1 |
Niemann-Pick Disease Type C2 (NPC2) | NPC2 |
Retinal Degeneration II | CEP290 |
Rickets Type 1B | CYP2R1 |
Rickets Type I 1, 2 | CYP27B1, CYP27B2 |
Rod-Cone Dysplasia | CRX |
Spasticity (Congenital Myasthenic Syndrome, CMS) | COLQ |
Spinal Muscular Atrophy | LIX1 |