Genetic testing required by breed
Genetic testing is necessary to ensure that our kittens will not acquire certain genetic diseases from their parents. The tests do not guarantee that a kitten is 100% safe from a certain disease, but that it is not transmitted by the parents.
Bengal
Progressive retinal atrophy (rdAc-PRA)
Progressive retinal atrophy (b-PRA)
Pyruvate kinase deficiency (PK Deficiency)
British Longhair
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Autoimmune lymphoproliferative syndrome (ALPS) *only for cats with Australian and New Zealand ancestry
British Shorthair
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Autoimmune lymphoproliferative syndrome (ALPS) *only for cats with Australian and New Zealand ancestry
Cornish Rex
Burmese Hypokalemia
Progressive retinal atrophy (pd-PRA)
Exotic
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Maine Coon
Hypertrophic cardiomyopathy (HCM)
Spinal muscular atrophy (SMA)
Pyruvate kinase deficiency (PK Deficiency)
Munchkin Longhair
Progressive retinal atrophy (rdAc-PRA)
Munchkin Shorthair
Progressive retinal atrophy (rdAc-PRA)
Norwegian Forest Cat
Pyruvate kinase deficiency (PK Deficiency)
Glycogen storage disease type IV (GSD4)
Oriental
Mucopolysaccharidosis type VI (MPS6)
Primary congenital glaucoma (PCG)
Korat Gangliosidosis (GM1)
Progressive retinal atrophy (rdAc-PRA)
Persian
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Alpha-Mannosidosis (AMD)
Ragdoll
Hypertrophic cardiomyopathy (HCM)
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Russian Blue
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Sacred Burmese
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Mucopolysaccharidosis type VI (MPS6)
Scottish Fold
Osteochondrodysplasia (OCD)
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Scottish Straight
Osteochondrodysplasia (OCD)
Polycystic kidney disease (PKD)
Progressive retinal atrophy (pd-PRA)
Siamese
Mucopolysaccharidosis type VI (MPS6)
Primary congenital glaucoma (PCG)
Korat Gangliosidosis (GM1)
Progressive retinal atrophy (rdAc-PRA)
Siberian
Pyruvate kinase deficiency (PK Deficiency)
Polycystic kidney disease (PKD)
Sphynx
Burmese Hypokalemia
Congenital myasthenic syndrome (CMS)
Hypertrophic cardiomyopathy (HCM)