Portie Club PWD's

Parent health testing

• Hip Dysplasia (rDVM, not registered)

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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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• Eye Examination (rDVM, not 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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• Cardiac Evaluation (registered with OFA)

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  Heart testing reduces the chance of passing down congenital heart disease, which can cause a range of symptoms ranging from trouble exercising to heart failure.

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• Temperament Test, Standard Veterinary Blood Panel

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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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• X-Linked Progressive Retinal Atrophy (XL-PRA), X-Linked Progressive Retinal Atrophy 2, X-Linked Progressive Retinal Atrophy 1, X-Linked Myotubular Myopathy, Wisdom Panel, von Willebrand Disease III (vWD III), Ullrich Congenital Muscular Dystrophy, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Thrombopathia (RASGRP2 Exon 8), Siberian Husky Shaking Puppy Syndrome, Type 1 (SPS1), Spongy Degeneration with Cerebellar Ataxia (SDCA2) mutation originally found in Belgian Shepherd Dog, Spongy Degeneration with Cerebellar Ataxia (SDCA1) mutation originally found in Belgian Shepherd Dog and Malinois, Spinal Dysraphism (SD), Spinocerebellar Ataxia (SCA), Skeletal Dysplasia (SD2), Severe Combined Immunodeficiency Disease, Frisian Water Dog Type, Retinal Dysplasia/Oculoskeletal Dysplasia 2, Sensory Neuropathy, Border Collie Type (SN), Retinal Dysplasia/Oculoskeletal Dysplasia 1 (RD OSD), Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Progressive Retinal Atrophy (PRA), Generalized, Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), PRA, Rod-Cone Dysplasia 4 (rcd4), PRA, Rod-Cone Dysplasia 3 (rcd3), PRA, Rod-Cone Dysplasia 2 (rcd2), PRA, Rod-Cone Degeneration (PRA-prcd), Primary Hyperoxaluria, Primary Lens Luxation (PLL), Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Polycystic Kidney Disease (PKD), Pituitary Dwarfism, Persistent Müllerian Duct Syndrome, P2RY12 Receptor Platelet Disorder, Oculocutaneous Albinism, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neonatal Encephalopathy with Seizures (NEwS), Neonatal Cortical Cerebellar Degeneration (NCCD), Narcolepsy, Labrador Retriever Type, Musladin-Leuke Syndrome (MLS), Mucopolysaccharidosis VI (MPS VI), Poodle Type, Malignant Hyperthermia (MH), Lundehund Syndrome, Long QT Syndrome, Ligneous Membranitis, LM (PLG), Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Lagotto Storage Disease (LSD), Juvenile Myoclonic Epilepsy (JME), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Inflammatory Myopathy (Myositis), Ichthyosis (KRY10), Hypocatalasia, Hereditary Vitamin D-Resistant Rickets (HVDRR), Hereditary (Juvenile) Cataracts (HC; JC), Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis, Hereditary Ataxia, Cerebellar Ataxia, GM2 Gangliosidosis, Poodle Type, GM1 Gangliosidosis, Alaskan Husky Type, Glycogen Storage Disease Ia, Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), Fanconi Syndrome, Factor XI Deficiency, Factor VII Deficiency, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Early Adult Onset Deafness (EAOD), Dry Eye Curly Coat Syndrome (CKSID), Diffuse cystic renal dysplasia and hepatic fibrosis, Dental-skeletal-retinal anomaly (DSRA), Degenerative Myelopathy (DM; SOD1A), Day Blindness, Achromatopsia, Cystinuria Type 1A, Newfoundland Type, Craniomandibular Osteopathy (CMO), Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Spanish Water Dog Type, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter (CHG), Centronuclear Myopathy (CNM), Cerebellar Degeneration, Cardiomyopathy and Juvenile Mortality (YARS2), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Bernard-Soulier Syndrome, Cocker Spaniel Type, Alanine Aminotransferase Activity, Bald Thigh Syndrome (IGFBP5), Early Onset Progressive Retinal Atrophy (EOPRA), Dominant Black DNA Test, D Locus (Dilute) DNA test, DNA Coat/Trait Panel, Dilated Cardiomyopathy 1 (DCM1), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Chondrodystrophy and IVDD Risk (CDDY-IVDD), PRA, Cone-Rod Dystrophy 1 (PRA-crd1), Optimal Selection Genetic Disease Analysis (180+ Diseases), Juvenile Dilated Cardiomyopathy, Genetic Diversity Test, GM1 Gangliosidosis, Portuguese Water Dog Type, DNA Disease Panel, Dilated Cardiomyopathy 2 (DCM2), Cleft Palate (ADAMTS20), Chondrodysplasia/Dwarfism, Animal Genetics Panel

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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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