Winsome Aussies

Parent health testing

• Hip Dysplasia

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  Hip testing reduces the chance of passing down hip dysplasia, which is primarily found in large breed dogs and can cause hip pain and the eventual loss of the function of the hip joint.

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• Elbow Dysplasia Finals (OFA, BVA, SV, FCI)

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  Elbow testing reduces the chance of passing down elbow dysplasia, which is primarily found in large breed dogs and can cause arthritis in the elbow joint and front leg lameness.

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• Eye Certification (CAER, registered with OFA)

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  Eye testing reduces the chance of passing down a wide range of hereditary eye illnesses including retinal dysplasia, lens luxation, and glaucoma, which can cause impared vision or blindness.

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• Canine Good Citizen (CGC)

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  A breeder may perform additional tests on their dogs that do not fall into these general categories. These tests may be more uncommon or very specific to a particular breed.

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• PawPrint Genetic Panel (Breed Specific), Multiple Drug Sensitivity (MDR1), Agouti DNA Test, Collie Eye Anomaly (CEA), Adult Paroxysmal Dyskinesia, Adult Onset Neuropathy (AON), Dilated Cardiomyopathy 1 (DCM1), Dilated Cardiomyopathy 2 (DCM2), Day Blindness, Achromatopsia, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter (CHG), Congenital Stationary Night Blindness (CSNB), Cystinuria Type 1A, Labrador Retriever Type, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Degenerative Myelopathy (DM; SOD1A), Exercise Induced Collapse (EIC), Full Embark Panel, Factor IX Deficiency, Airedale Terrier Type, Factor IX Deficiency, Rhodesian Ridgeback Type, Factor VII Deficiency, Scottish Deerhound Type, Factor VIII Deficiency, Boxer Type, Factor VIII Deficiency (Exon 1), German Shepherd Type, Factor VIII Deficiency (Exon 11), German Shepherd Type, Gangliosidosis GM2, Japanese Chin Type, GM2 Gangliosidosis, Poodle Type, GM1 Gangliosidosis, Alaskan Husky Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, Hereditary Nasal Parakeratosis (HNPK), Hypocatalasia, Hypomyelination, Weimaraner Type, Hereditary Ataxia, Cerebellar Ataxia, Hyperuricosuria (HUU), Ichthyosis, German Shepherd Type, Ichthyosis, American Bulldog Type, Inherited Myopathy in Great Danes (IMGD), Ichthyosis (KRY10), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Juvenile Myoclonic Epilepsy (JME), DNA Profile, Cleft Palate (ADAMTS20), Osteogenesis Imperfecta (OI), Chow Chow Type, Osteogenesis Imperfecta (OI), Beagle Type, Osteogenesis Imperfecta (OI), Golden Retriever Type, X-Linked Progressive Retinal Atrophy (XL-PRA), X-Linked Anhidrotic Ectodermal Dysplasia, Dachshund type, von Willebrand Disease I (vWD I), von Willebrand Disease II (vWD II) (RESEARCH ONLY), von Willebrand Disease III (vWD III), Scottish Terrier Type, von Willebrand Disease III (vWD III), Kooikerhondje Type, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Skeletal Dysplasia (SD2), Severe Combined Immunodeficiency Disease, Terrier Type, Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Polyneuropathy (NDRG1), Alaskan Malamute Type, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, P2RY12 Receptor Platelet Disorder, Progressive Retinal Atrophy (PRA), Generalized

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  Genetic testing reduces the chance of passing down a wide variety of hereditary diseases of differing prevalence and severity such as Progressive Retinal Atrophy (an eye disease) and Von Willebrand's Disease (a blood disease).

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