$ 119.95
Easily identify the genetic conditions that can impact your cat’s health, all in a single test – INCLUDES CAT PERSONALIZED LIFEPLAN™
説明
[vc_row][vc_column][vc_column_text]This is great value profile that includes all cat diseases and traits in a single test. The Cat Health Screen also include a personalized LifePlan™ and a schedule you may follow with your veterinarian to implement a customized wellness plan for your pet.
What’s in the Kit?
- Sterile DNA Collection Swabs
- Information Brochure with DNA Collection Instructions
- Self Addressed Pre-Paid Envelope
How Do I Get My Results?
Results are presented in an interactive online account where you can constantly update your pet’s records such as weight, body condition, nutrition, health records and medication. Your account will also give you access to special promotions and attractive offers via your very own personalized shop. You can easily share your pet’s profile with your veterinarian, health care providers, family and friends.
[/vc_column_text][vc_column_text]Includes the following
- 6. Cat Life Plan
- Acute Intermitent Porphyria
- Agouti
- Albinism – Siamese
- Alpha Mannisidosis
- Amber
- Blood Groups
- Cat DNA Health Screen & Life Plan
- Chocolate & Cinnamon
- Chylomicronemia (Lipoprotein Lipase Deficiency)
- Colourpoint Restriction (Siamese/Burmese)
- Curly Coat – Cornish Rex
- Curly Coat – Selkirk Rex
- Cystinuria (SLC3A1)
- Devon Rex Coat
- Dilute
- GM1 – Gangliosidosis
- Glycogen Storage Disease Type IV
- Haemophilia B
- Hereditary Retinal Degeneration PRA (CEP290)
- Hyperoxaluria (GRHPR)
- Hypertrophic Cardiomyopathy – Maine Coon
- Hypertrophic Cardiomyopathy – Ragdoll
- Hypokalaemia Periodic Polymyopathy – Burmese
- Lipoprotein Deficiency (LPL)
- Long Hair / Short Hair
- Mucopolysaccharidosis Type I
- Mucopolysaccharidosis Type VI (D520N) NO ASSOCIATION (MILD FORM)
- Mucopolysaccharidosis Type VI (L467P) – SEVERE FORM
- Myopathy (COLQ)
- Myotonia Congenita (Feline)
- Neurodegenerative Lysosomal Storage Disease
- Niemann-Pick Disease – Sphingomyelinosis
- Polycystic Kidney Disease
- Preaxial Polydactyl
- Pyruvate Kinase Deficiency (Feline)
- Sphynx (KRT71 Variant)
- Spinal Muscular Atrophy
- Vitamin D Rickets
- White Gloves (Birman Pattern)